Nucleic acid molecules and other molecules associated with the carbon assimilation pathway

ABSTRACT

The present invention is in the field of plant biochemistry. More specifically the invention relates to nucleic acid sequences from plant cells, in particular, nucleic acid sequences from maize and soybean associated with the carbon assimilation pathway enzymes. The invention encompasses nucleic acid molecules that encode proteins and fragments of proteins. In addition, the invention also encompasses proteins and fragments of proteins so encoded and antibodies capable of binding these proteins or fragments. The invention also relates to methods of using the nucleic acid molecules, proteins and fragments of proteins and antibodies, for example for genome mapping, gene identification and analysis, plant breeding, preparation of constructs for use in plant gene expression and transgenic plants.

CROSS REFERENCE TO RELATED APPLICATIONS

This application claims priority under 35 U.S.C. § 119(e) of application No. 60/076,712 filed Mar. 6, 1998, the entirety of which is herein incorporated by reference.

FIELD OF THE INVENTION

The present invention is in the field of plant biochemistry. More specifically the invention relates to nucleic acid sequences from plant cells, in particular, nucleic acid sequences from maize and soybean plants associated with the carbon assimilation pathway in plants. The invention encompasses nucleic acid molecules that encode proteins and fragments of proteins. In addition, the invention also encompasses proteins and fragments of proteins so encoded and antibodies capable of binding these proteins or fragments. The invention also relates to methods of using the nucleic acid molecules, proteins and fragments of proteins and antibodies, for example for genome mapping, gene identification and analysis, plant breeding, preparation of constructs for use in plant gene expression and transgenic plants.

BACKGROUND OF THE INVENTION I. Introduction

The primary sites of photosynthetic activity, generally referred to as “source organs”, are mature leaves and to a lesser extent, other green tissues (e.g., stems). Photosynthesis may be broadly divided into two phases: a light phase, in which the electromagnetic energy of sunlight is trapped and converted into ATP and NADPH, and a dark or synthetic phase, in which the ATP and NADPH generated by the light phase are used, in part, for biosynthetic carbon reduction. In most plants, the major products of photosynthesis are starch (transitory storage form of carbohydrate formed in chloroplasts), and sucrose (formed in the cytosol). Sucrose represents the predominant form of carbon transport in higher plants. Processes that play a role in plant growth and development, crop yield potential and stability, and crop quality and composition include: enhanced carbon assimilation, efficient carbon storage, and increased carbon export and partitioning.

Oxygen-evolving organisms are reported to have a common pathway for the reduction of CO₂ to sugar phosphates. This pathway is known as the reductive pentose phosphate (RPP), Calvin-Benson or C3 cycle (Calvin and Bassham, The Photosynthesis of Carbon Compounds, Benjamin, New York (1962); Bassham and Buchanan, In: Photosynthesis, Govindjee, ed., Academic Press, New York, 141-189 (1982), both of which are herein incorporated by reference). A number of plants exhibit adaptations in which CO₂ is first fixed by a supplementary pathway and then released in cells in which the RPP cycle operates. From the point of view of the metabolic pathway operating for photosynthetic carbon assimilation, higher plants can be classified by the existence of supplemental pathway such as C3, C4, and crassulacean acid metabolism species (Edwards and Walker, C3-C4: Mechanism and cellular and environmental regulation ofphotosynthesis, Blackwell Scientific Publications, Oxford, (1983), herein incorporated by reference in its entirety).

The RPP pathway is reported to be the main route by which CO₂ is ultimately incorporated into organic compounds in all species of higher plants (Edwards and Walker, C3-C4: Mechanism and cellular and environmental regulation ofphotosynthesis, Blackwell Scientific Publications, Oxford, (1983); Macdonald and Buchanan, In: Plant Physiology, Biochemistry and Molecular Biology, Dennis and Turpin, eds., J. Wiley & Sons, Inc., New York, p. 239 (1990), herein incorporated by reference in its entirety; Robinson and Walker, In: The Biochemistry of Plants, Vol. 8, Hatch and Boardman, eds., Academic Press, New York, p. 193 (1981), herein incorporated by reference in its entirety). In C3 plants, the RPP pathway is the sole route for photosynthetic carbon assimilation, whereas in C4 and CAM plants an additional (not alternative) method of carbon fixation, is present separated in space (C4 plants) or in time (CAM plants) from the RPP cycle (Edwards and Walker, C3-C4: Mechanism and cellular and environmental regulation ofphotosynthesis, Blackwell Scientific Publications, Oxford, (1983)). Carbon skeletons are required to incorporate other functional groups, the operation of the RPP cycle for photosynthetic CO₂ fixation is a requisite for the biochemical synthesis of carbohydrates, lipids, proteins, and nucleic acids.

II. The Reductive Pentose Phosphate Cycle

The RPP cycle is reported to be the primary carboxylating mechanism in plants. Enzymes which catalyze steps in the RPP cycle are water soluble and are located in the soluble portion of the chloroplast (stroma). Reviews on the mechanism and enzymes involved in the RPP cycle include: Bhagwat, In: Handbook of Photosynthesis, Pessaraki, ed., Marcel Dekker Inc, New York, 461-480 (1997), herein incorporated by reference in its entirety; Iglesias et al., In: Handbook of Photosynthesis, Pessaraki, ed., Marcel Dekker Inc, New York, 481-503 (1997), herein incorporated by reference in its entirety; Robinson and Walker, In: The Biochemistry of Plants, Vol. 8, Hatch and Boardman, eds., Academic Press, New York, 193-236 (1981); Macdonald and Buchanan, In: Plant Metabolism, Dennis et al., eds., Longman, Essex, England, 299-313 (1997).

The RPP pathway is an autocatalytic pathway for the de novo synthesis of carbohydrates from inorganic CO₂. The RPP cycle is reported to comprise three phases. The first phase of the cycle is the carboxylation phase, during which ribulose-1,5-bisphosphate (Rbu-1,5-P₂) is carboxylated to produce two molecules of 3-phosphoglycerate (3-PGA). The next phase is the reductive phase during which ATP and NADPH produced by the light reaction of photosynthesis are consumed in the reduction of 3-PGA to glyceraldehyde-3-phosphate (GA-3-P). The RPP cycle is completed by the regeneration phase where intermediates formed from GA-3-P are utilized via a series of isomerizations, condensations and rearrangements, resulting in the conversion of five molecules of triose phosphate to three molecules of pentose phosphate, and eventually ribulose 5-phosphate (Rbu-5-P). Phosphorylation of Rbu-5-P by ATP regenerates the original carbon acceptor Rbu-1,5-P₂, thus completing the cycle.

The RPP cycle is a metabolic pathway common to all photosynthetic organisms. Many of the enzymes of the metabolic route, as well as proteins involved in metabolite transport and regulation, have been purified.

Ribulose bisphosphate carboxylase (Rubisco, also referred to as ribulose-1,5-bisphosphate carboxylase/oxygenase (EC 4.1.1.39)) constitutes about 50% of the total soluble protein in green leaves. Ribulose bisphosphate carboxylase is reported to provide a quantitative link between the pools of inorganic and organic carbon in the biosphere. Ribulose bisphosphate carboxylase catalyses the conversion of atmospheric carbon dioxide into three carbon compounds. Subsequent reactions result in both regeneration of the acceptor molecule and translocation of three molecules of triose-phosphate to the cytosol for synthesis of sucrose and starch. Reviews of the ribulose bisphosphate carboxylase enzyme are provided by Ellis, Trends Biochem. Sci. 4: 241-244 (1979); Hartman and Harpel, Annu. Rev. Biochem. 63: 197-234 (1994); Miziorko and Lorimer, Annu. Rev. Biochem. 52: 507-535 (1983); Andrews and Lorimer, In: The Biochemistry of Plants, Vol 10, Hatch and Boardman, eds., Academic Press, San Diego, p. 131 (1987); Jensen, In: Plant Physiology, Biochemistry, and Molecular Biology, Dennis and Turpin, eds., J. Wiley & Sons, Inc., New York, p 224 (1990), all of which are herein incorporated by reference in their entirety.

Plants are reported to have two phosphoglycerate kinase isoenzymes (EC 2.7.2.3), one in the chloroplast and the other in the cytosol. The two isoenzymes are antigenically related, but can be distinguished on the basis of their isoelectric point (pI) values and on the basis of their affinity for magnesium and other substrates (Anderson and Advani, Plant Physiol. 45:583-585 (1970); Kopke-Secundo et al., Plant Physiol. 93:40-47 (1990), both of which are herein incorporated by reference in their entirety).

Three different glyceraldehyde 3-phosphate dehydrogenase (GAPDH (EC 1.2.1.13)) enzymes are found in eukaryotic cells (Pupillo and Faggiani, Arch. Biochem. Biophys. 194: 581-592 (1979); Iglesias, Biochem. Educ. 18: 2-5 (1990), both of which are herein incorporated by reference in their entirety). In higher plants there are two chloroplast GAPDH subunits: GapA (36 kDa) and GapB (42 kDa). The functional enzyme is reported to be a tetramer with either an A₄ or an A₂B₂ subunit structure (Cerff, In: Methods in Choroplast Molecular Biology, Edelman, ed., Elsevier Press, Amsterdam: 683 (1982), the entirety of which is herein incorporated by reference). Sequence analysis of tobacco cDNA clones encoding the GapA and GapB subunits has revealed that they are homologous (Shih et al., Cell 47: 73-83 (1986), the entirety of which is herein incorporated by reference). The three-dimensional structure of GADPH from both eukaryotes and prokaryotes has been studied, and it seems that the initial binding of the NAD coenzyme triggers a number of structural changes (Skarzynski and Wonacott, J. Mol. Biol. 203: 1097-1118 (1988), the entirety of which is herein incorporated by reference).

Chloroplastic triose phosphate isomerase (TPI (EC 5.3.1.1)) is a homodimer with a subunit molecular weight of about 27 kDa (Pichersky and Gottlieb, Plant Physiol. 74: 340-347 (1984), the entirety of which is herein incorporated by reference). The chloroplastic enzyme is reported to be distinguishable from the cytosolic enzyme by isoelectric focusing and peptide digestion mapping (Pichersky and Gottlieb, Plant Physiol. 74: 340-347 (1984); Kurzok and Feierabend, Biochim. Biophys. Acta 788: 222-233 (1984), herein incorporated by reference in its entirety). TPI, like several other RPP cycle enzymes, binds the substrate in a pocket, which is then reported to be closed by a flexible loop which acts to shield the substrate from attack by water. Even though the active site is formed by residues from one subunit, the second subunit helps to exclude water from the active site domain.

Two reactions of the RPP cycle involve aldolase (EC 4.1.2.13), and both are catalyzed by the same enzyme, which is a tetramer of the 38 kDa subunit. It has been reported that each subunit of aldolase has a beta/alpha barrel structure (Sygusch et al., Proc. Natl. Acad. Sci. (U.S.A.) 84:7846-7850 (1987), the entirety of which is herein incorporated by reference) and that the C-terminal region covers the active site pocket, which is in the barrel and regulates access to the active site pocket.

Fructose-1,6-bisphosphatase (FBPase) (EC 3.1.3.11) is a homotetramer with a molecular weight of about 160 kDa. The amino acid sequence is reported to be highly conserved (Raines et al., Nucleic Acid Res. 16: 7931-7942 (1988), the entirety of which is herein incorporated by reference). In both wheat and spinach, 12 extra amino acid residues have been identified that seem to be involved in the regulation by light via the ferredoxin/thioredoxin system (Raines et al., Nucleic Acid Res. 16: 7931-7942 (1988); Marcus et al., Proc. Natl. Acad. Sci. (U.S.A.) 85:5379-5383 (1988), the entirety of which is herein incorporated by reference).

Transketolase (EC 2.2.1.1) (152 kDa tetramer) is found in cytosolic and chloroplastic forms. These forms are reported to have similar properties except for their response to Mg²⁺(Feierbend and Gringel, Zeitschrift fur Pflanzenphysiol. 110:247-258 (1983); Murphy and Walker, Planta 155: 316-320 (1982), both of which are herein incorporated by reference in their entirety).

Sedoheptulose-1,7-bisphosphate phosphatase (SBPase (EC 3.1.3.37)) is not reported to have a cytosolic counterpart and is reported to be found only in the chloroplast. The enzyme is reported to be a homodimer with a subunit molecular weight of 35-38 kDa (Nishizawa and Buchanan, J. Biol. Chem. 256: 6119-6126 (1981); Cadet and Meunier, Biochem. J. 253: 243-248 (1988), both of which are herein incorporated by reference in their entirety).

D-ribulose-5-phosphate-3-epimerase (EC 5.1.3.1) has been reported in animals as a homodimer with a subunit molecular weight of 23 kDa (Karmali et al., Biochem. J. 211:617-623 (1983), the entirety of which is herein incorporated by reference).

Ribose-5-phosphate isomerase (EC 5.3.1.6) has been purified from tobacco and spinach and is reported to be a homodimer with a subunit molecular weight of 26 kDa (Rutner, Biochemistry 9: 178-184 (1970); Babadzhanova and Bakaeva, Biokhimiya 53: 134-140 (1987), both of which are herein incorporated by reference in their entirety).

III. Regulation of C3 Photosynthesis

The regulatory properties of the RPP cycle have been reported by Edwards and Walker, C3-C4: Mechanism and Cellular and Environmental Regulation of Photosynthesis, Blackwell Scientific Publications, Oxford, (1983); Leegood, Photosynthesis Res. 6: 247-259 (1985), herein incorporated by reference in its entirety; Woodrow, Biochim. Biophys. Acta 851:181-192 (1986), the entirety of which is herein incorporated by reference. The conservation of phosphate is reported to play a role in the regulation of C3 photosynthesis, as a change in the level of any phosphorylated intermediate is balanced by an equal and opposite change in terms of phosphate elsewhere in the cycle (Woodrow, Biochim. Biophys. Acta. 851:181-192 (1986); Fell and Sauro, Eur. J. Biochem. 148: 555-561 (1985), herein incorporated by reference in its entirety). Therefore, changes in the activity of any of the RPP cycle enzymes can affect both the substrate concentration and activities of other enzymes in the chloroplast.

IV. The C4 Pathway of Carbon Assimilation

In the C4 pathway, CO₂ is concentrated in bundle sheath cells at the site of the RPP cycle initiated by ribulose bisphosphate carboxylase. C3 photosynthesis is documented to be the only mode of carbon assimilation in algae, bryophytes, pteridophytes, gymnosperms, and the majority of angiosperm families. Only about 10 families of known monocots and dicots have been reported to possess the C4 pathway of photosynthesis, these include, for example, Zea mays, sorghum, sugar cane, etc. The C4 pathway has been reviewed by, for example, Edwards et al., In: CO ₂ Metabolism and Productivity of Plants, Burris and Black, eds., University Park Press, Baltimore, Md., p. 83 (1976); Hatch, Biochim. Biophys. Acta 895: 81-106 (1987); Ashton et al., In: Methods In Plant Biochemistry, Vol. 3, Academic Press Limited, New York, p. 39 (1990), all of which are herein incorporated by reference in their entirety. A feature reported to be common to the enzymes in the C4 pathway is that their activities are 15-100 times higher compared to those reported in C3 plants. For example, adenylate kinase and pyrophosphatase activities are reported to be 20-50 times higher in C4 plants than in C-3 plants. Adenylate kinase and pyrophosphatase are largely located in the mesophyll chloroplast together with pyruvate Pi dikinase (Slack et al., Biochem. J. 114: 489-498 (1969), herein incorporated by reference in its entirety).

In certain plant types (e.g., Zea mays, sorghum and sugar cane), CO₂ is initially assimilated in mesophyll cells (with PEP acting as a primary acceptor of CO₂) as oxaloacetate, which is reduced to malate by NADP-malate dehydrogenase. It has been reported that malate is moved to bundle sheath cells. In the chloroplast of bundle sheath cells, malate is decarboxylated by NADP-malic enzyme (malate formers) giving rise to pyruvate, and releasing CO₂ and NADPH. NADPH can be cycled back to NADP by coupling to PGA reduction in the RPP cycle. The carbon formed moves back to the mesophyll cells where it is converted to PEP by pyruvate Pi dikinase.

Plants of the PEP carboxykinase type are reported to have higher activities of aspartate and alanine aminotransferases than the malate formers. Such plants are reported to be aspartate formers rather than malate formers. In aspartate formers, the activity of PEP carboxykinase is reported to be higher and the activity of NADP-malic enzyme is reported to be lower (Edwards and Black, In: Photosynthesis and Photorespiration, Hatch et al., eds., Wiley Interscience, New York, p. 153 (1971), the entirety of which is herein incorporated by reference). It has been reported that the PEP carboxykinase is located in the cytosol of bundle sheath cells.

This group of C4 plants is not reported to contain either high levels of NAD-malic enzyme activity or high levels of PEP carboxykinase. It has been reported by Hatch and Kagawa (Aust. J. Plant Physiol. 1: 357-369 (1974), the entirety of which is herein incorporated by reference) that these plants contain high NAD-malic enzyme activity in mitochondria and that the number of mitochondria in these plants may be increased by a factor of 3-4.

V. Enzymes Involved in the C4 Pathway

Phosphoenolpyruvate carboxylase (PEP carboxykinase (EC 4.1.1.31)) is reported to initiate the carboxylative phase of the C4 metabolic route by catalyzing the irreversible beta-carboxylation of PEP. The reaction utilizes a divalent metal ion (e.g., Mg²⁺) as a cofactor. In C4 plants, PEP carboxykinase is reported to play a role in catalyzing the initial fixation of atmospheric CO₂ in the cytoplasm of mesophyll cells (O'Leary, Annu. Rev. Plant Physiol. 33: 297-315 (1982); Andreo et al., FEBS Lett. 213: 1-8 (1987), both of which are herein incorporated by reference in their entirety). PEP carboxykinase from C4 plants is reported to be a homotetramer with molecular weight of 400 kDa (O'Leary, Annu. Rev. Plant Physiol. 33: 297-315 (1982); Andreo et al., FEBS Lett. 213: 1-8 (1987)). Each subunit is reported to contain at least one substrate-binding site. The monomeric form is reported to be inactive (Wagner et al., Eur. J. Biochem. 173: 561-568 (1988); Walker et al., Plant Physiol. 80: 848-855 (1986); Wagner et al., Eur. J. Biochem. 164: 661-666 (1987), all of which are herein incorporated by reference in their entirety).

In C4 plants, PEP carboxykinase is reported to be allosterically regulated. Glucose-6-phosphate, triose-phosphate and Pi are reported to be activators, and malate is reported to be an inhibitor of enzyme activity. C4 PEP carboxykinase is also reported to be subject to light regulation. Responses to light/dark involve a post-translational modification of the enzyme (Jiao and Chollet, Plant Physiol. 95: 981 (1991), herein incorporated by reference in its entirety). The PEP carboxykinase is phosphorylated, during the light phase, at a serine residue close to the N-terminal region of the enzyme (Ser-15 in Zea mays) (Jiao and Chollet, Plant Physiol. 95: 981 (1991)). The phosphorylation is reported to be catalyzed by a soluble protein-serine kinase. The phosphorylated form of PEP carboxykinase is reported to be less sensitive to malate inhibition.

NADP-dependent malate dehydrogenase (NADP-MDHase (EC 1.1.1.82)) is reported to be located in the chloroplast of mesophyll cells and is reported to reduce oxaloacetate (OAA) by using photosynthetically generated NADPH. The native enzyme is reported to be a dimer composed of a nuclear-encoded subunit of molecular mass 42 kDa (Jenkins et al., Plant Sci. 45: 1-7 (1986); Kagawa and Bruno, Arch. Biochem. Biophys. 260: 674-695 (1988), both of which are herein incorporated by reference in their entirety). In C4 plants, NADP-MDHase is reported to have an alkaline pH optimum and the reduction of OAA is reported to be inhibited by NADP+. NADP-MDHase is reported to be light regulated with the enzyme active during the light phase and inactive during the dark phase. The activation mechanism involves reversible thiol/disulfide interchanges mediated by ferredoxin and thioredoxin m. The reaction is promoted under conditions of high NADPH:NADP+ ratio in the chloroplast stroma.

Aspartate aminotransferase (EC 2.6.1.1) is a cytoplasmic enzyme that converts OAA and glutamate into aspartate and alpha-ketoglutarate (alpha-KG) in mesophyll cells (Taniguchi et al., Arch. Biochem. Biophys. 282: 427-432 (1990); Rastogi et al., J. Bacteriol. 173: 2879-2887 (1991); Reynolds et al., Plant Mol. Biol. 19: 465-472 (1992); Kirk et al., Plant Physiol. 105: 763-764 (1994); Schultz et al., Plant J. 7: 61-75 (1995), all of which are herein incorporated by reference in their entirety). Aspartate is exported into bundle sheath cells where decarboxylation takes place. Aspartate aminotransferase is reported to be present in aspartate forming C4 plants.

Alanine aminotransferase (EC 2.6.1.2) is reported to be present in C4 plants of the NAD-dependent malic acid enzyme (NAD-ME) type and interconverts in a reversible reaction the metabolites pyruvate and alanine in the cytoplasm of both mesophyll and bundle sheath cells (Son et al., Plant Mol. Biol. 20: 705-713 (1992); Umemura et al., Biosci. Biotechnol. Biochem. 58: 283-287 (1994), both of which are herein incorporated by reference in their entirety). The amino acid alanine is a metabolite transported in this C4 subtype.

NADP-dependent malic enzyme (NADP-ME (EC 1.1.1.40)) is reported to be present in NADP-ME type C4 plants and is located in the chloroplasts of bundle sheath cells. NADP-ME catalyses the conversion of malate into pyruvate and CO₂ in the presence of NADP+. This reaction is reported to require a metal ion (Ashton et al., In: Methods in Plant Biochemistry, Lea, ed., Academic Press, New York, p. 39 (1990); Leegood and Osmond, In: Plant Physiology, Biochemistry and Molecular Biology, Dennis and Turpin, eds., Wiley & Sons, Inc., New York, p. 274 (1990), herein incorporated by reference in its entirety). The NADP-ME enzyme in C4 plants is reported to comprise a single subunit with molecular weight of 62 kDa. At least two plastidic isoforms of NADP-ME, “dark” form and “light” form (the light form is also know as the “green” form), have been reported in Zea mays leaves (Andreo et al., In: Proceedings of the International Congress on Photosynthesis, Montepelier, France, Mathis, ed., Kluwer Academic Publishers, Amsterdam, (1995), the entirety of which is herein incorporated by reference). The dark form of the NADP-ME, which is present mainly in etiolated Zea mays leaves, has a molecular weight of 72 kDa and a lower specific activity compared to the “green” form of NADP-ME (62 kDa) found in green leaves (Andreo et al., In: Proceedings of the International Congress on Photosynthesis, Montepelier, France, Mathis, ed., Kluwer Academic Publishers, Amsterdam, (1995)). The “green” form of NADP-ME appears to be enhanced by light. The dark form of the enzyme resembles the NADP-MEs found in C-3 plants in both photosynthetic and nonphotosynthetic tissues.

NAD-dependent malic enzyme (NAD-ME (EC 1.1.1.39)) is reported to be located in the mitochondria where it catalyzes the NAD-dependent decarboxylation of malate in the presence of a divalent cation (e.g., Mg²⁺). NAD-ME is reported to be ineffective in the decarboxylation of OAA (Artus and Edwards, FEBS Lett. 182: 225-233 (1985), the entirety of which is herein incorporated by reference). NAD-ME is reported to comprise two subunits (alpha and beta) which differ in molecular weights (58 and 62 kDa, respectively).

In C4 plants of the PEP carboxykinase (EC 4.1.1.49) type, aspartate is converted into OAA in bundle sheath cells and ketoacid is decarboxylated by cytoplasmic PEP carboxykinase. PEP carboxykinase is reported to have a requirement for Mn²⁺ and a preference for ATP (Ashton et al., In: Methods in Plant Biochemistry, Lea, ed., Academic Press, New York, p. 39 (1990)). The native enzyme is reported to be a homohexamer with a molecular weight of 380 kDa (subunit molecular weight of 64 kDa). PEP carboxykinase enzyme is reported to be inhibited by the metabolites 3PGA, fructose-6-phosphate, fructose1,6 bisphosphate and DHAP.

In all three subtypes of C4 plants, regeneration of PEP from pyruvate takes place in mesophyll chloroplasts by the reaction catalyzed by pyruvate Pi dikinase (PPDKase (EC 2.7.9.1)). This is a regulatory step in the C4 pathway (Hatch, Biochim. Biophys. Acta 895: 81-106 (1987); Ashton et al., In: Methods in Plant Biochemistry, Lea, ed., Academic Press, New York, p. 39 (1990)). PPDKase is a homotetrameric protein with a molecular weight of about 390 kDa (Ashton et al., In: Methods in Plant Biochemistry, Lea, ed., Academic Press, New York, p. 39 (1990)). PPDKase is reported to be inactivated by cold temperatures and the absence of Mg²⁺ and is activated in the light period and inactivated in the dark period ((Ashton et al., In: Methods in Plant Biochemistry, Lea, ed., Academic Press, New York, p. 39 (1990)). Activation by light of PPDKase is a result of dephosphorylation and the switch to inactive dark form involves phosphorylation.

Pyrophosphatase (inorganic pyrophosphatase (EC 3.6.1.1)) promotes the reaction catalyzed by the enzyme pyruvate Pi dikinase in the direction of PEP synthesis through hydrolysis of PPi (Jiang et al., Arch. Biochem. Biophys. 346: 105-112 (1997); Mitchell et al., Can. J. Microbiol. 43: 734-743 (1997), both of which are herein incorporated by reference in their entirety). Pyrophosphatase has been isolated from potato (du Jardin et al., Plant Physiol 109:853-860 (1995), herein incorporated by reference in its entirety) and Arabidopisis (Kieber and Signer, Plant Mol. Biol. 16: 345-348 (1991), herein incorporated by reference in its entirety).

Ribose-5-phosphate kinase (EC 2.7.1.19) is reported to be found in photosynthetic organisms possessing the C-4 pathway. This homodimeric enzyme has a subunit molecular weight of 39.2 kDa (Roeslier and Ogren, Nucleic Acid Res. 16: 7192 (1988); Milanez and Mural, Gene 66:55-63 (1988), both of which are herein incorporated by reference in their entirety). The N-terminal region seems to be involved in the regulation of catalytic activity. Cys¹⁶ may form a part of the ATP-binding region. Lys⁶⁸ has also been implicated in ATP binding (Miziorko et al., J. Biol. Chem. 265: 3642-3647 (1990), the entirety of which is herein incorporated by reference).

VI. Expressed Sequence Tag Nucleic Acid Molecules

Expressed sequence tags, or ESTs are randomly sequenced members of a cDNA library (or complementary DNA)(McCombie et al., Nature Genetics 1:124-130 (1992); Kurata et al., Nature Genetics 8:365-372 (1994); Okubo et al., Nature Genetics 2:173-179 (1992), all of which references are incorporated herein in their entirety). The randomly selected clones comprise insets that can represent a copy of up to the full length of a mRNA transcript.

Using conventional methodologies, cDNA libraries can be constructed from the mRNA (messenger RNA) of a given tissue or organism using poly dT primers and reverse transcriptase (Efstratiadis et al., Cell 7:279-3680 (1976), the entirety of which is herein incorporated by reference; Higuchi et al., Proc. Natl. Acad. Sci. (U.S.A.) 73:3146-3150 (1976), the entirety of which is herein incorporated by reference; Maniatis et al., Cell 8:163-182 (1976) the entirety of which is herein incorporated by reference; Land et al., Nucleic Acids Res. 9:2251-2266 (1981), the entirety of which is herein incorporated by reference; Okayama et al., Mol. Cell. Biol. 2:161-170 (1982), the entirety of which is herein incorporated by reference; Gubler et al., Gene 25:263-269 (1983), the entirety of which is herein incorporated by reference).

Several methods may be employed to obtain full-length cDNA constructs. For example, terminal transferase can be used to add homopolymeric tails of dC residues to the free 3′ hydroxyl groups (Land et al, Nucleic Acids Res. 9:2251-2266 (1981), the entirety of which is herein incorporated by reference). This tail can then be hybridized by a poly dG oligo which can act as a primer for the synthesis of full length second strand cDNA. Okayama and Berg, Mol. Cell. Biol. 2:161-170 (1982), the entirety of which is herein incorporated by reference, report a method for obtaining full length cDNA constructs. This method has been simplified by using synthetic primer-adapters that have both homopolymeric tails for priming the synthesis of the first and second strands and restriction sites for cloning into plasmids (Coleclough et al., Gene 34:305-314 (1985), the entirety of which is herein incorporated by reference) and bacteriophage vectors (Krawinkel et al., Nucleic Acids Res. 14:1913 (1986), the entirety of which is herein incorporated by reference; Han et al., Nucleic Acids Res. 15:6304 (1987), the entirety of which is herein incorporated by reference).

These strategies have been coupled with additional strategies for isolating rare mRNA populations. For example, a typical mammalian cell contains between 10,000 and 30,000 different mRNA sequences (Davidson, Gene Activity in Early Development, 2nd ed., Academic Press, New York (1976), the entirety of which is herein incorporated by reference). The number of clones required to achieve a given probability that a low-abundance mRNA will be present in a cDNA library is N=(ln(1−P))/(ln(1−1/n)) where N is the number of clones required, P is the probability desired and 1/n is the fractional proportion of the total mRNA that is represented by a single rare mRNA (Sambrook et al., Molecular Cloning: A Laboratory Manual, 2nd ed., Cold Spring Harbor Laboratory Press (1989), the entirety of which is herein incorporated by reference).

A method to enrich preparations of mRNA for sequences of interest is to fractionate by size. One such method is to fractionate by electrophoresis through an agarose gel (Pennica et al., Nature 301:214-221 (1983), the entirety of which is herein incorporated by reference). Another such method employs sucrose gradient centrifugation in the presence of an agent, such as methylmercuric hydroxide, that denatures secondary structure in RNA (Schweinfest et al., Proc. Natl. Acad. Sci. (U.S.A.) 79:4997-5000 (1982), the entirety of which is herein incorporated by reference).

A frequently adopted method is to construct equalized or normalized cDNA libraries (Ko, Nucleic Acids Res. 18:5705-5711 (1990), the entirety of which is herein incorporated by reference; Patanjali et al., Proc. Natl. Acad. Sci. (U.S.A.) 88:1943-1947 (1991), the entirety of which is herein incorporated by reference). Typically, the cDNA population is normalized by subtractive hybridization (Schmid et al., J. Neurochem. 48:307-312 (1987), the entirety of which is herein incorporated by reference; Fargnoli et al., Anal. Biochem. 187:364-373 (1990), the entirety of which is herein incorporated by reference; Travis et al., Proc. Natl. Acad. Sci. (U.S.A.) 85:1696-1700 (1988), the entirety of which is herein incorporated by reference; Kato, Eur. J. Neurosci. 2:704-711 (1990); and Schweinfest et al., Genet. Anal. Tech. Appl. 7:64-70 (1990), the entirety of which is herein incorporated by reference). Subtraction represents another method for reducing the population of certain sequences in the cDNA library (Swaroop et al., Nucleic Acids Res. 19:1954 (1991), the entirety of which is herein incorporated by reference).

ESTs can be sequenced by a number of methods. Two basic methods may be used for DNA sequencing, the chain termination method of Sanger et al., Proc. Natl. Acad. Sci. (U.S.A.) 74:5463-5467 (1977), the entirety of which is herein incorporated by reference and the chemical degradation method of Maxam and Gilbert, Proc. Nat. Acad. Sci. (U.S.A.) 74:560-564 (1977), the entirety of which is herein incorporated by reference. Automation and advances in technology such as the replacement of radioisotopes with fluorescence-based sequencing have reduced the effort required to sequence DNA (Craxton, Methods 2:20-26 (1991), the entirety of which is herein incorporated by reference; Ju et al., Proc. Natl. Acad. Sci. (U.S.A.) 92:4347-4351 (1995), the entirety of which is herein incorporated by reference; Tabor and Richardson, Proc. Natl. Acad. Sci. (U.S.A.) 92:6339-6343 (1995), the entirety of which is herein incorporated by reference). Automated sequencers are available from, for example, Pharmacia Biotech, Inc., Piscataway, N.J. (Pharmacia ALF), LI-COR, Inc., Lincoln, Nebr. (LI-COR 4,000) and Millipore, Bedford, Mass. (Millipore BaseStation).

In addition, advances in capillary gel electrophoresis have also reduced the effort required to sequence DNA and such advances provide a rapid high resolution approach for sequencing DNA samples (Swerdlow and Gesteland, Nucleic Acids Res. 18:1415-1419 (1990); Smith, Nature 349:812-813 (1991); Luckey et al., Methods Enzymol. 218:154-172 (1993); Lu et al., J. Chromatog. A. 680:497-501 (1994); Carson et al., Anal. Chem. 65:3219-3226 (1993); Huang et al., Anal. Chem. 64:2149-2154 (1992); Kheterpal et al., Electrophoresis 17:1852-1859 (1996); Quesada and Zhang, Electrophoresis 17:1841-1851 (1996); Baba, Yakugaku Zasshi 117:265-281 (1997), all of which are herein incorporated by reference in their entirety).

ESTs longer than 150 nucleotides have been found to be useful for similarity searches and mapping (Adams et al., Science 252:1651-1656 (1991), herein incorporated by reference). ESTs, which can represent copies of up to the full length transcript, may be partially or completely sequenced. Between 150-450 nucleotides of sequence information is usually generated as this is the length of sequence information that is routinely and reliably produced using single run sequence data. Typically, only single run sequence data is obtained from the cDNA library (Adams et al., Science 252:1651-1656 (1991). Automated single run sequencing typically results in an approximately 2-3% error or base ambiguity rate (Boguski et al., Nature Genetics 4:332-333 (1993), the entirety of which is herein incorporated by reference).

EST databases have been constructed or partially constructed from, for example, C. elegans (McCombrie et al., Nature Genetics 1: 124-131 (1992)), human liver cell line HepG2 (Okubo et al., Nature Genetics 2:173-179 (1992)), human brain RNA (Adams et al., Science 252:1651-1656 (1991); Adams et al., Nature 355:632-635 (1992)), Arabidopsis, (Newman et al., Plant Physiol. 106:1241-1255 (1994)); and rice (Kurata et al., Nature Genetics 8:365-372 (1994)).

VII. Sequence Comparisons

A characteristic feature of a DNA sequence is that it can be compared with other DNA sequences. Sequence comparisons can be undertaken by determining the similarity of the test or query sequence with sequences in publicly available or proprietary databases (“similarity analysis”) or by searching for certain motifs (“intrinsic sequence analysis”)(e.g. cis elements)(Coulson, Trends in Biotechnology 12:76-80 (1994), the entirety of which is herein incorporated by reference); Birren et al., Genome Analysis 1: Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. 543-559 (1997), the entirety of which is herein incorporated by reference).

Similarity analysis includes database search and alignment. Examples of public databases include the DNA Database of Japan (DDBJ) (http://www.ddbj.nig.ac.jp/); Genebank (http://www.ncbi.nlm.nih.gov/Web/Search/Index.htlm); and the European Molecular Biology Laboratory Nucleic Acid Sequence Database (EMBL) (http://www.ebi.ac.uk/ebi_docs/embl_db/embl-db.html). Other appropriate databases include dbEST (http://www.ncbi.nlm.nih.gov/dbEST/index.html), SwissProt (http://www.ebi.ac.uk/ebi_docs/swisprot_db/swisshome.html), PIR (http://www-nbrt.georgetown.edu/pir/) and The Institute for Genome Research (http://www.tigr.org/tdb/tdb.html)

A number of different search algorithms have been developed, one example of which are the suite of programs referred to as BLAST programs. There are five implementations of BLAST, three designed for nucleotide sequences queries (BLASTN, BLASTX and TBLASTX) and two designed for protein sequence queries (BLASTP and TBLASTN) (Coulson, Trends in Biotechnology 12:76-80 (1994); Birren et al., Genome Analysis 1, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. 543-559 (1997)).

BLASTN takes a nucleotide sequence (the query sequence) and its reverse complement and searches them against a nucleotide sequence database. BLASTN was designed for speed, not maximum sensitivity and may not find distantly related coding sequences. BLASTX takes a nucleotide sequence, translates it in three forward reading frames and three reverse complement reading frames and then compares the six translations against a protein sequence database. BLASTX is useful for sensitive analysis of preliminary (single-pass) sequence data and is tolerant of sequencing errors (Gish and States, Nature Genetics 3:266-272 (1993), the entirety of which is herein incorporated by reference). BLASTN and BLASTX may be used in concert for analyzing EST data (Coulson, Trends in Biotechnology 12:76-80 (1994); Birren et al., Genome Analysis 1:543-559 (1997)).

Given a coding nucleotide sequence and the protein it encodes, it is often preferable to use the protein as the query sequence to search a database because of the greatly increased sensitivity to detect more subtle relationships. This is due to the larger alphabet of proteins (20 amino acids) compared with the alphabet of nucleic acid sequences (4 bases), where it is far easier to obtain a match by chance. In addition, with nucleotide alignments, only a match (positive score) or a mismatch (negative score) is obtained, but with proteins, the presence of conservative amino acid substitutions can be taken into account. Here, a mismatch may yield a positive score if the non-identical residue has physical/chemical properties similar to the one it replaced. Various scoring matrices are used to supply the substitution scores of all possible amino acid pairs. A general purpose scoring system is the BLOSUM62 matrix (Henikoff and Henikoff, Proteins 17:49-61 (1993), the entirety of which is herein incorporated by reference), which is currently the default choice for BLAST programs. BLOSUM62 is tailored for alignments of moderately diverged sequences and thus may not yield the best results under all conditions. Altschul, J. Mol. Biol. 36:290-300 (1993), the entirety of which is herein incorporated by reference, describes a combination of three matrices to cover all contingencies. This may improve sensitivity, but at the expense of slower searches. In practice, a single BLOSUM62 matrix is often used but others (PAM40 and PAM250) may be attempted when additional analysis is necessary. Low PAM matrices are directed at detecting very strong but localized sequence similarities, whereas high PAM matrices are directed at detecting long but weak alignments between very distantly related sequences.

Homologues in other organisms are available that can be used for comparative sequence analysis. Multiple alignments are performed to study similarities and differences in a group of related sequences. CLUSTAL W is a multiple sequence alignment package that performs progressive multiple sequence alignments based on the method of Feng and Doolittle, J. Mol. Evol. 25:351-360 (1987), the entirety of which is herein incorporated by reference. Each pair of sequences is aligned and the distance between each pair is calculated; from this distance matrix, a guide tree is calculated and all of the sequences are progressively aligned based on this tree. A feature of the program is its sensitivity to the effect of gaps on the alignment; gap penalties are varied to encourage the insertion of gaps in probable loop regions instead of in the middle of structured regions. Users can specify gap penalties, choose between a number of scoring matrices, or supply their own scoring matrix for both pairwise alignments and multiple alignments. CLUSTAL W for UNIX and VMS systems is available at: ftp.ebi.ac.uk. Another program is MACAW (Schuler et al., Proteins Struct. Func. Genet. 9:180-190 (1991), the entirety of which is herein incorporated by reference, for which both Macintosh and Microsoft Windows versions are available. MACAW uses a graphical interface, provides a choice of several alignment algorithms and is available by anonymous ftp at: ncbi.nlm.nih.gov (directory/pub/macaw).

Sequence motifs are derived from multiple alignments and can be used to examine individual sequences or an entire database for subtle patterns. With motifs, it is sometimes possible to detect distant relationships that may not be demonstrable based on comparisons of primary sequences alone. Currently, the largest collection of sequence motifs in the world is PROSITE (Bairoch and Bucher, Nucleic Acid Research 22:3583-3589 (1994), the entirety of which is herein incorporated by reference). PROSITE may be accessed via either the ExPASy server on the World Wide Web or anonymous ftp site. Many commercial sequence analysis packages also provide search programs that use PROSITE data.

A resource for searching protein motifs is the BLOCKS E-mail server developed by Henikoff, Trends Biochem Sci. 18:267-268 (1993), the entirety of which is herein incorporated by reference; Henikoff and Henikoff, Nucleic Acid Research 19:6565-6572 (1991), the entirety of which is herein incorporated by reference; Henikoff and Henikoff, Proteins 17:49-61 (1993). BLOCKS searches a protein or nucleotide sequence against a database of protein motifs or “blocks.” Blocks are defined as short, ungapped multiple alignments that represent highly conserved protein patterns. The blocks themselves are derived from entries in PROSITE as well as other sources. Either a protein query or a nucleotide query can be submitted to the BLOCKS server; if a nucleotide sequence is submitted, the sequence is translated in all six reading frames and motifs are sought for these conceptual translations. Once the search is completed, the server will return a ranked list of significant matches, along with an alignment of the query sequence to the matched BLOCKS entries.

Conserved protein domains can be represented by two-dimensional matrices, which measure either the frequency or probability of the occurrences of each amino acid residue and deletions or insertions in each position of the domain. This type of model, when used to search against protein databases, is sensitive and usually yields more accurate results than simple motif searches. Two popular implementations of this approach are profile searches such as GCG program ProfileSearch and Hidden Markov Models (HMMs) (Krough et al., J. Mol. Biol. 235:1501-1531, (1994); Eddy, Current Opinion in Structural Biology 6:361-365, (1996), both of which are herein incorporated by reference in their entirety). In both cases, a large number of common protein domains have been converted into profiles, as present in the PROSITE library, or HHM models, as in the Pfam protein domain library (Sonnhammer et al., Proteins 28:405-420 (1997), the entirety of which is herein incorporated by reference). Pfam contains more than 500 HMM models for enzymes, carbon assimilation pathway enzymes, signal transduction molecules and structural proteins. Protein databases can be queried with these profiles or HMM models, which will identify proteins containing the domain of interest. For example, HMMSW or HMMFS, two programs in a public domain package called HMMER (Sonnhammer et al., Proteins 28:405-420 (1997)) can be used.

PROSITE and BLOCKS represent collected families of protein motifs. Thus, searching these databases entails submitting a single sequence to determine whether or not that sequence is similar to the members of an established family. Programs working in the opposite direction compare a collection of sequences with individual entries in the protein databases. An example of such a program is the Motif Search Tool, or MoST (Tatusov et al., Proc. Natl. Acad. Sci. (U.S.A.) 91:12091-12095 (1994), the entirety of which is herein incorporated by reference). On the basis of an aligned set of input sequences, a weight matrix is calculated by using one of four methods (selected by the user). A weight matrix is simply a representation, position by position of how likely a particular amino acid will appear. The calculated weight matrix is then used to search the databases. To increase sensitivity, newly found sequences are added to the original data set, the weight matrix is recalculated and the search is performed again. This procedure continues until no new sequences are found.

SUMMARY OF THE INVENTION

The present invention provides a substantially purified nucleic acid molecule that encodes a maize or soybean carbon assimilation pathway enzyme or fragment thereof, wherein the maize or soybean carbon assimilation pathway enzyme is selected from the group consisting of: (a) ribulose-bisphosphate carboxylase; (b) phosphoglycerate kinase; (c) glyceraldehyde 3-phosphate dehydrogenase; (d) putative glyceraldehyde 3-phosphate dehydrogenase; (e) triose phosphate isomerase; (f) aldolase; (g) fructose-1,6-bisphosphatase; (h) transketolase; (i) putative transketolase; (j) sedoheptulose-1,7-bisphophatase; (k) D-ribulose-5-phosphate-3-epimerase; (l) ribose-5-phosphate isomerase; (m) putative ribose-5-phosphate isomerase; (n) ribose-5-phosphate kinase; (o) phosphoenolpyruvate carboxylase; (p) NADP-dependent malate dehydrogenase; (q) aspartate aminotransferase; (r) putative aspartate aminotransferase; (s) alanine aminotransferase; (t) NADP-dependent malec enzyme; (u) NAD-dependent malic enzyme; (v) PEP carboxykinase; (w) putative PEP carboxykinase; (x) pyruvate, phosphate dikinase; and (y) pyrophosphatase.

The present invention also provides a substantially purified nucleic acid molecule that encodes a plant carbon assimilation pathway enzyme or fragment thereof, wherein the nucleic acid molecule is selected from the group consisting of a nucleic acid molecule that encodes a maize or soybean ribulose-bisphosphate carboxylase or fragment thereof, a nucleic acid molecule that encodes a maize or soybean phosphoglycerate kinase or fragment thereof, a nucleic acid molecule that encodes a maize or soybean glyceraldehyde 3-phosphate dehydrogenase or fragment thereof, a nucleic acid molecule that encodes a putative maize glyceraldehyde 3-phosphate dehydrogenase or fragment thereof, a nucleic acid molecule that encodes a maize or soybean triose phosphate isomerase or fragment thereof, a nucleic acid molecule that encodes a maize or soybean aldolase or fragment thereof, a nucleic acid molecule that encodes a maize or soybean fructose-1,6-bisphosphatase or fragment thereof, a nucleic acid molecule that encodes a maize or soybean transketolase or fragment thereof, a nucleic acid molecule that encodes a putative maize or soybean transketolase or fragment thereof, a nucleic acid molecule that encodes a maize or soybean sedoheptulose-1,7-bisphophatase or fragment thereof, a nucleic acid molecule that encodes a maize or soybean D-ribulose-5-phosphate-3-epimerase or fragment thereof, a nucleic acid molecule that encodes a maize or soybean ribose-5-phosphate isomerase or fragment thereof, a nucleic acid molecule that encodes a putative maize or soybean ribose-5-phosphate isomerase or fragment thereof, a nucleic acid molecule that encodes a maize or soybean ribose-5-phosphate kinase or fragment thereof, a nucleic acid molecule that encodes a maize or soybean phosphoenolpyruvate carboxylase or fragment thereof, a nucleic acid molecule that encodes a maize or soybean NADP-dependent malate dehydrogenase or fragment thereof, a nucleic acid molecule that encodes a maize or soybean aspartate aminotransferase or fragment thereof, a nucleic acid molecule that encodes a putative maize or soybean aspartate aminotransferase or fragment thereof, a nucleic acid molecule that encodes a maize or soybean alanine aminotransferase or fragment thereof, a nucleic acid molecule that encodes a maize or soybean NADP-dependent malic enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean NAD-dependent malic enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean PEP carboxykinase or fragment thereof, a nucleic acid molecule that encodes a putative soybean PEP carboxykinase or fragment thereof, a nucleic acid molecule that encodes a maize or soybean pyruvate, phosphate dikinase or fragment thereof and a nucleic acid molecule that encodes a maize or soybean pyrophospatase or fragment thereof.

The present invention also provides a substantially purified maize or soybean carbon assimilation pathway enzyme or fragment thereof, wherein the maize or soybean carbon assimilation pathway enzyme is selected from the group consisting of (a) ribulose-bisphosphate carboxylase or fragment thereof; (b) phosphoglycerate kinase; (c) glyceraldehyde 3-phosphate dehydrogenase; (d) putative glyceraldehyde 3-phosphate dehydrogenase; (e) triose phosphate isomerase; (f) aldolase; (g) fructose-1,6-bisphosphatase; (h) transketolase; (i) putative transketolase; (j) sedoheptulose-1,7-bisphophatase; (k) D-ribulose-5-phosphate-3-epimerase; (l) ribose-5-phosphate isomerase; (m) putative ribose-5-phosphate isomerase; (n) ribose-5-phosphate kinase; (o) phosphoenolpyruvate carboxylase; (p) NADP-dependent malate dehydrogenase; (q) aspartate aminotransferase; (r) putative aspartate aminotransferase; (s) alanine aminotransferase; (t) NADP-dependent malic enzyme; (u) NAD-dependent malic enzyme; (v) PEP carboxykinase; (w) putative PEP carboxykinase; (x) pyruvate, phosphate dikinase; and (y) pyrophosphatase.

The present invention also provides a substantially purified maize or soybean carbon assimilation pathway enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 1 through SEQ ID NO: 7341.

The present invention also provides a substantially purified maize or soybean ribulose-bisphosphate carboxylase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 1 through SEQ ID NO: 281 and SEQ ID NO: 282 through SEQ ID NO: 847.

The present invention also provides a substantially purified maize or soybean ribulose-bisphosphate carboxylase enzyme or fragment thereof encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 281 and SEQ ID NO: 282 through SEQ ID NO: 847.

The present invention also provides a substantially purified maize or soybean phosphoglycerate kinase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 848 through SEQ ID NO: 1090 and SEQ ID NO: 1091 through SEQ ID NO: 1307.

The present invention also provides a substantially purified maize or soybean phosphoglycerate kinase enzyme or fragment thereof encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NO: 848 through SEQ ID NO: 1090 and SEQ ID NO: 1091 through SEQ ID NO: 1307.

The present invention also provides a substantially purified maize or soybean glyceraldehyde 3-phosphate dehydrogenase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence consisting of a complement of SEQ ID NO: 1308 through SEQ ID NO: 2383 and SEQ ID NO: 2397 through SEQ ID NO: 3540.

The present invention also provides a substantially purified maize or soybean glyceraldehyde 3-phosphate dehydrogenase enzyme or fragment thereof encoded by a nucleic acid sequence consisting of SEQ ID NO: 1308 through SEQ ID NO: 2383 and SEQ ID NO: 2397 through SEQ ID NO: 3540.

The present invention also provides a substantially purified putative maize glyceraldehyde 3-phosphate dehydrogenase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence consisting of a complement of SEQ ID NO: 2384 through SEQ ID NO: 2396.

The present invention also provides a substantially purified putative maize glyceraldehyde 3-phosphate dehydrogenase enzyme or fragment thereof encoded by a nucleic acid sequence consisting of SEQ ID NO: 2384 through SEQ ID NO: 2396.

The present invention also provides a substantially purified maize or soybean triose phosphate isomerase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 3541 through SEQ ID NO: 3746 and SEQ ID NO: 3747 through SEQ ID NO: 3918.

The present invention also provides a substantially purified maize or soybean triose phosphate isomerase enzyme or fragment thereof encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NO: 3541 through SEQ ID NO: 3746 and SEQ ID NO: 3747 through SEQ ID NO: 3918.

The present invention also provides a substantially purified maize or soybean aldolase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 3919 through SEQ ID NO: 3963 and SEQ ID NO: 3964 through SEQ ID NO: 4370.

The present invention also provides a substantially purified maize or soybean aldolase enzyme or fragment thereof encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NO: 3919 through SEQ ID NO: 3963 and SEQ ID NO: 3964 through SEQ ID NO: 4370.

The present invention also provides a substantially purified maize or soybean fructose-1,6-bisphosphatase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 4371 through SEQ ID NO: 4421 and SEQ ID NO: 4422 through SEQ ID NO: 4475.

The present invention also provides a substantially purified soybean fructose-1,6-bisphosphatase enzyme or fragment thereof encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NO: 4371 through SEQ ID NO: 4421 and SEQ ID NO: 4422 through SEQ ID NO: 4475.

The present invention also provides a substantially purified maize or soybean transketolase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 4476 through SEQ ID NO: 4513 and SEQ ID NO: 4525 through SEQ ID NO: 4605.

The present invention also provides a substantially purified maize or soybean transketolase or fragment thereof encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NO: 4476 through SEQ ID NO: 4513 and SEQ ID NO: 4525 through SEQ ID NO: 4605.

The present invention also provides a substantially purified putative maize or soybean transketolase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 4514 through SEQ ID NO: 4524 and SEQ ID NO: 4606 through SEQ ID NO: 4612.

The present invention also provides a substantially purified putative maize or soybean transketolase or fragment thereof encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NO: 4514 through SEQ ID NO: 4524 and SEQ ID NO: 4606 through SEQ ID NO: 4612.

The present invention also provides a substantially purified maize or soybean sedoheptulose-1,7-bisphophatase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 4613 through SEQ ID NO: 4614 and SEQ ID NO: 4615 through SEQ ID NO: 4677.

The present invention also provides a substantially purified maize or soybean sedoheptulose-1,7-bisphosphatase enzyme or fragment thereof encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NO: 4613 through SEQ ID NO: 4614 and SEQ ID NO: 4615 through SEQ ID NO: 4677.

The present invention also provides a substantially purified maize or soybean D-ribulose-5-phosphate-3-epimerase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 4678 through SEQ ID NO: 4723 and SEQ ID NO: 4724 through SEQ ID NO 4762.

The present invention also provides a substantially purified maize or soybean D-ribulose-5-phosphate-3-epimerase enzyme or fragment thereof encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NO: 4678 through SEQ ID NO: 723 and SEQ ID NO: 4724 through SEQ ID NO 4762.

The present invention also provides a substantially purified maize or soybean ribose-5-phosphate isomerase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence consisting of a complement of SEQ ID NO: 4763 through SEQ ID NO: 4769 and SEQ ID NO: 4772 through SEQ ID NO: 4776.

The present invention also provides a substantially purified maize or soybean ribose-5-phosphate isomerase enzyme or fragment thereof encoded by a nucleic acid sequence consisting of SEQ ID NO: 4763 through SEQ ID NO: 4769 and SEQ ID NO: 4772 through SEQ ID NO: 4776.

The present invention also provides a substantially purified putative maize or soybean ribose-5-phosphate isomerase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence consisting of a complement of SEQ ID NO: 4770 through SEQ ID NO: 4771 and SEQ ID NO: 4777 through SEQ ID NO: 4781.

The present invention also provides a substantially purified putative maize or soybean ribose-5-phosphate isomerase enzyme or fragment thereof encoded by a nucleic acid sequence consisting of SEQ ID NO: 4770 through SEQ ID NO: 4771 and SEQ ID NO: 4777 through SEQ ID NO: 4781.

The present invention also provides a substantially purified maize or soybean ribose-5-phosphate kinase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 4782 through SEQ ID NO: 4832 and SEQ ID NO: 4833 through SEQ ID NO: 4908.

The present invention also provides a substantially purified maize or soybean ribose-5-phosphate kinase enzyme or fragment thereof encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NO: 4782 through SEQ ID NO: 4832 and SEQ ID NO: 4833 through SEQ ID NO: 4908.

The present invention also provides a substantially purified maize or soybean phosphoenolpyruvate carboxylase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 4909 through SEQ ID NO: 5282 and SEQ ID NO: 5283 through SEQ ID NO: 5371.

The present invention also provides a substantially purified maize or soybean phosphoenolpyruvate enzyme or fragment thereof encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NO: 4909 through SEQ ID NO: 5282 and SEQ ID NO: 5283 through SEQ ID NO: 5371.

The present invention also provides a substantially purified maize or soybean NADP-dependent malate dehydrogenase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 5372 through SEQ ID NO: 5419 and SEQ ID NO: 5420 through SEQ ID NO: 5423.

The present invention also provides a substantially purified soybean NADP-dependent malate dehydrogenase enzyme or fragment thereof encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NO: 5372 through SEQ ID NO: 5419 and SEQ ID NO: 5420 through SEQ ID NO: 5423.

The present invention also provides a substantially purified maize or soybean aspartate aminotransferase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 5424 through SEQ ID NO: 5596 and SEQ ID NO: 5601 through SEQ ID NO: 5719.

The present invention also provides a substantially purified maize or soybean aspartate aminotransferase enzyme or fragment thereof encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NO: 5424 through SEQ ID NO: 5596 and SEQ ID NO: 5601 through SEQ ID NO: 5719.

The present invention also provides a substantially purified putative maize or soybean aspartate aminotransferase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 5597 through SEQ ID NO: 5600 and SEQ ID NO: 5720 through SEQ ID NO: 5727.

The present invention also provides a substantially purified putative maize or soybean aspartate aminotransferase enzyme or fragment thereof encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NO: 5597 through SEQ ID NO: 5600 and SEQ ID NO: 5720 through SEQ ID NO: 5727.

The present invention also provides a substantially purified maize or soybean alanine aminotransferase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 5728 through SEQ ID NO: 5888 and SEQ ID NO: 5889 through SEQ ID NO: 6004.

The present invention also provides a substantially purified maize or soybean alanine aminotransferase enzyme or fragment thereof encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NO: 5728 through SEQ ID NO: 5888 and SEQ ID NO: 5889 through SEQ ID NO: 6004.

The present invention also provides a substantially purified maize or soybean NADP-dependent malic enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 6005 through SEQ ID NO: 6223 and SEQ ID NO: 6224 through SEQ ID NO: 6287.

The present invention also provides a substantially purified maize or soybean NADP-dependent malic enzyme or fragment thereof encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NO: 6005 through SEQ ID NO: 6223 and SEQ ID NO: 6224 through SEQ ID NO: 6287.

The present invention also provides a substantially purified maize or soybean NAD-dependent malic enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence consisting of a complement of SEQ ID NO: 6022 through SEQ ID NO: 6023, SEQ ID NO: 6288 through SEQ ID NO: 6290 and SEQ ID NO: 6291 through SEQ ID NO: 6293.

The present invention also provides a substantially purified maize or soybean NAD-dependent malic enzyme or fragment thereof encoded by a nucleic acid sequence consisting of SEQ ID NO: 6022 through SEQ ID NO: 6023, SEQ ID NO: 6288 through SEQ ID NO: 6290 and SEQ ID NO: 6291 through SEQ ID NO: 6293.

The present invention also provides a substantially purified maize or soybean PEP carboxykinase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 6294 through SEQ ID NO: 6353 and SEQ ID NO: 6354 through SEQ ID NO: 6387.

The present invention also provides a substantially purified maize or soybean PEP carboxykinase enzyme or fragment thereof encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NO: 6294 through SEQ ID NO: 6353 and SEQ ID NO: 6354 through SEQ ID NO: 6387.

The present invention also provides a substantially purified putative soybean PEP carboxykinase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence consisting of a complement of SEQ ID NO: 6388.

The present invention also provides a substantially purified putative soybean PEP carboxykinase enzyme or fragment thereof encoded by a nucleic acid sequence consisting of SEQ ID NO: 6388.

The present invention also provides a substantially purified maize or soybean pyruvate, phosphate dikinase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 6389 through SEQ ID NO: 6847 and SEQ ID NO: 6848 through SEQ ID NO: 6850.

The present invention also provides a substantially purified maize or soybean pyruvate, phosphate dikinase enzyme or fragment thereof encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NO: 6389 through SEQ ID NO: 6847 and SEQ ID NO: 6848 through SEQ ID NO: 6850.

The present invention also provides a substantially purified maize or soybean pyrophosphatase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 6851 through SEQ ID NO: 7154 and SEQ ID NO: 7155 through SEQ ID NO: 7341.

The present invention also provides a substantially purified soybean pyrophosphates enzyme or fragment thereof encoded by a nucleic acid sequence selected from the group consisting of SEQ ID NO: 6851 through SEQ ID NO: 7154 and SEQ ID NO: 7155 through SEQ ID NO: 7341.

The present invention also provides a purified antibody or fragment thereof which is capable of specifically binding to a maize or soybean carbon assimilation pathway enzyme or fragment thereof, wherein the maize or soybean or carbon assimilation pathway enzyme or fragment thereof is encoded by a nucleic acid molecule comprising a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341.

The present invention also provides a substantially purified antibody or fragment thereof, the antibody or fragment thereof capable of specifically binding to a maize or soybean ribulose-bisphosphate carboxylase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 1 through SEQ ID NO: 281 and SEQ ID NO: 282 through SEQ ID NO: 847.

The present invention also provides a substantially purified antibody or fragment thereof, the antibody or fragment thereof capable of specifically binding to a maize or soybean phosphoglycerate kinase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 848 through SEQ ID NO: 1090 and SEQ ID NO: 1091 through SEQ ID NO: 1307.

The present invention also provides a substantially purified antibody or fragment thereof, the antibody or fragment thereof capable of specifically binding to a maize or soybean glyceraldehyde 3-phosphate dehydrogenase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule consisting of a compliment of a nucleic acid sequence having a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1308 through SEQ ID NO: 2383 and SEQ ID NO: 2397 through SEQ ID NO: 3540

The present invention also provides a substantially purified antibody or fragment thereof, the antibody or fragment thereof capable of specifically binding to a putative maize glyceraldehyde 3-phosphate dehydrogenase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule consisting of a compliment of a nucleic acid sequence having a nucleic acid sequence selected from the group consisting of SEQ ID NO: 2384 through SEQ ID NO: 2396.

The present invention also provides a substantially purified antibody or fragment thereof, the antibody or fragment thereof capable of specifically binding to a maize or soybean triose phosphate isomerase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 3541 through SEQ ID NO: 3746 and SEQ ID NO: 3747 through SEQ ID NO: 3918.

The present invention also provides a substantially purified antibody or fragment thereof, the antibody or fragment thereof capable of specifically binding to a maize or soybean aldolase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 3919 through SEQ ID NO: 3963 and SEQ ID NO: 3964 through SEQ ID NO: 4370.

The present invention also provides a substantially purified antibody or fragment thereof, the antibody or fragment thereof capable of specifically binding to a maize or soybean fructose-1,6-bisphosphatase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 4371 through SEQ ID NO: 4421 and SEQ ID NO: 4422 through SEQ ID NO: 4475.

The present invention also provides a substantially purified antibody or fragment thereof, the antibody or fragment thereof capable of specifically binding to a maize or soybean transketolase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 4476 through SEQ ID NO: 4513 and SEQ ID NO: 4525 through SEQ ID NO: 4605.

The present invention also provides a substantially purified antibody or fragment thereof, the antibody or fragment thereof capable of specifically binding to a putative maize or soybean transketolase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 4514 through SEQ ID NO: 4524 and SEQ ID NO: 4606 through SEQ ID NO: 4612.

The present invention also provides a substantially purified antibody or fragment thereof, the antibody or fragment thereof capable of specifically binding to a maize or soybean sedoheptulose-1,7-bisphosphatase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 4613 through SEQ ID NO: 4614 and SEQ ID NO: 4615 through SEQ ID NO: 4677.

The present invention also provides a substantially purified antibody or fragment thereof, the antibody or fragment thereof capable of specifically binding to a maize or soybean D-ribulose-5-phosphate-3-epimerase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 4678 through SEQ ID NO: 4723 and SEQ ID NO: 4724 through SEQ ID NO: 4762.

The present invention also provides a substantially purified antibody or fragment thereof, the antibody or fragment thereof capable of specifically binding to a maize or soybean ribose-5-phosphate isomerase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 4763 through SEQ ID NO: 4769 and SEQ ID NO: 4772 through SEQ ID NO: 4776.

The present invention also provides a substantially purified antibody or fragment thereof, the antibody or fragment thereof capable of specifically binding to a putative maize or soybean ribose-5-phosphate isomerase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 4770 through SEQ ID NO: 4771 and SEQ ID NO: 4777 through SEQ ID NO: 4781.

The present invention also provides a substantially purified antibody or fragment thereof, the antibody or fragment thereof capable of specifically binding to a maize or soybean ribose-5-phosphate kinase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 4782 through SEQ ID NO: 4832 and SEQ ID NO: 4833 through SEQ ID NO: 4908.

The present invention also provides a substantially purified antibody or fragment thereof, the antibody or fragment thereof capable of specifically binding to a maize or soybean phosphoenolpyruvate carboxylase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 4909 through SEQ ID NO: 5282 and SEQ ID NO: 5283 through SEQ ID NO: 5371.

The present invention also provides a substantially purified antibody or fragment thereof, the antibody or fragment thereof capable of specifically binding to a maize or soybean NADP-dependent malate dehydrogenase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 5372 through SEQ ID NO: 5419 and SEQ ID NO: 5420 through SEQ ID NO: 5423.

The present invention also provides a substantially purified antibody or fragment thereof, the antibody or fragment thereof capable of specifically binding to a maize or soybean aspartate aminotransferase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 5424 through SEQ ID NO: 5596 and SEQ ID NO: 5601 through SEQ ID NO: 5719.

The present invention also provides a substantially purified antibody or fragment thereof, the antibody or fragment thereof capable of specifically binding to a putative maize or soybean aspartate aminotransferase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 5597 through SEQ ID NO: 5600 and SEQ ID NO: 5720 through SEQ ID NO: 5727.

The present invention also provides a substantially purified antibody or fragment thereof, the antibody or fragment thereof capable of specifically binding to a maize or soybean alanine aminotransferase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 5728 through SEQ ID NO: 5888 and SEQ ID NO: 5889 through SEQ ID NO: 6004.

The present invention also provides a substantially purified antibody or fragment thereof, the antibody or fragment thereof capable of specifically binding to a maize or soybean NADP-dependent malic enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule consisting of a compliment of a nucleic acid sequence having a nucleic acid sequence selected from the group consisting of SEQ ID NO: 6005 through SEQ ID NO: 6223 and SEQ ID NO: 6224 through SEQ ID NO: 6287.

The present invention also provides a substantially purified antibody or fragment thereof, the antibody or fragment thereof capable of specifically binding to a maize or soybean NAD-dependent malic enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 6022 through SEQ ID NO: 6023, SEQ ID NO: 6288 through SEQ ID NO: 6290 and SEQ ID NO: 6291 through SEQ ID NO: 6293.

The present invention also provides a substantially purified antibody or fragment thereof, the antibody or fragment thereof capable of specifically binding to a maize or soybean PEP carboxykinase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 6294 through SEQ ID NO: 6353 and SEQ ID NO: 6354 through SEQ ID NO: 6387.

The present invention also provides a substantially purified antibody or fragment thereof, the antibody or fragment thereof capable of specifically binding to a putative soybean PEP carboxykinase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence consisting of a complement of SEQ ID NO: 6388.

The present invention also provides a substantially purified antibody or fragment thereof, the antibody or fragment thereof capable of specifically binding to a maize or soybean pyruvate, phosphate dikinase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 6389 through SEQ ID NO: 6847 and SEQ ID NO: 6848 through SEQ ID NO: 6850.

The present invention also provides a substantially purified antibody or fragment thereof, the antibody or fragment thereof capable of specifically binding to a maize or soybean pyrophosphatase enzyme or fragment thereof encoded by a first nucleic acid molecule which specifically hybridizes to a second nucleic acid molecule, the second nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a complement of SEQ ID NO: 6851 through SEQ ID NO: 7154 and SEQ ID NO: 7155 through SEQ ID NO: 7341.

The present invention also provides a transformed plant having a nucleic acid molecule which comprises: (A) an exogenous promoter region which functions in a plant cell to cause the production of a mRNA molecule; (B) a structural nucleic acid molecule comprising a nucleic acid sequence selected from the group consisting of (a) a nucleic acid sequence which encodes for a maize or soybean ribulose-bisphosphate carboxylase enzyme or fragment thereof; (b) a nucleic acid sequence which encodes for a maize or soybean phosphoglycerate kinase enzyme or fragment thereof; (c) a nucleic acid sequence which encodes for a maize or soybean glyceraldehyde 3-phosphate dehydrogenase enzyme or fragment thereof; (d) a nucleic acid sequence which encodes for a putative maize glyceraldehyde 3-phosphate dehydrogenase enzyme or fragment thereof; (e) a nucleic acid sequence which encodes for a maize or soybean triose phosphate isomerase enzyme or fragment thereof; (f) a nucleic acid sequence which encodes for a maize or soybean aldolase enzyme or fragment thereof; (g) a nucleic acid sequence which encodes for a maize or soybean fructose-1,6-bisphosphatase enzyme or fragment thereof; (h) a nucleic acid sequence which encodes for a maize or soybean transketolase enzyme or fragment thereof; (i) a nucleic acid sequence which encodes for a putative maize or soybean transketolase enzyme or fragment thereof; (j) a nucleic acid sequence which encodes for a maize or soybean sedoheptulose-1,7-bisphophatase enzyme or fragment thereof; (k) a nucleic acid sequence which encodes for a maize or soybean D-ribulose-5-phosphate-3-epimerase enzyme or fragment thereof; (l) a nucleic acid sequence which encodes for a maize or soybean ribose-5-phosphate isomerase enzyme or fragment thereof; (m) a nucleic acid sequence which encodes for a putative maize or soybean ribose-5-phosphate isomerase enzyme or fragment thereof; (n) a nucleic acid sequence which encodes for a maize or soybean ribose-5-phosphate kinase enzyme or fragment thereof; (o) a nucleic acid sequence which encodes for a maize or soybean phosphoenolpyruvate dehydrogenase enzyme or fragment thereof; (p) a nucleic acid sequence which encodes for a maize or soybean NADP-dependent malate dehydrogenase enzyme or fragment thereof; (q) a nucleic acid sequence which encodes for a maize or soybean aspartate aminotransferase enzyme or fragment thereof; (r) a nucleic acid sequence which encodes for a putative maize or soybean aspartate aminotransferase enzyme or fragment thereof; (s) a nucleic acid sequence which encodes for a maize or soybean alanine aminotransferase enzyme or fragment thereof; (t) a nucleic acid sequence which encodes for a maize or soybean NADP-dependent malic enzyme or fragment thereof; (u) a nucleic acid sequence which encodes for a maize or soybean NAD-dependent malic enzyme or fragment thereof; (v) a nucleic acid sequence which encodes for a maize or soybean PEP carboxykinase enzyme or fragment thereof; (w) a nucleic acid sequence which encodes for a putative soybean PEP carboxykinase enzyme or fragment thereof; (x) a nucleic acid sequence which encodes for a maize or soybean pyruvate, phosphate dikinase enzyme or fragment thereof; and (y) a nucleic acid sequence which encodes for a maize or soybean pyrophosphatase enzyme or fragment thereof; (z) a nucleic acid sequence which is complementary to any of the nucleic acid sequences of (a) through (y); and (C) a 3′ non-translated sequence that functions in the plant cell to cause termination of transcription and addition of polyadenylated ribonucleotides to a 3′ end of the mRNA molecule.

The present invention also provides a transformed plant having a nucleic acid molecule which comprises: (A) an exogenous promoter region which functions in a plant cell to cause the production of a mRNA molecule; which is linked to (B) a structural nucleic acid molecule, wherein the structural nucleic acid molecule encodes a plant carbon assimilation pathway enzyme or fragment thereof, the structural nucleic acid molecule comprising a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341 or fragment thereof; which is linked to (C) a 3′ non-translated sequence that functions in the plant cell to cause termination of transcription and addition of polyadenylated ribonucleotides to a 3′ end of the mRNA molecule.

The present invention also provides a transformed plant having a nucleic acid molecule which comprises: (A) an exogenous promoter region which functions in a plant cell to cause the production of a mRNA molecule; which is linked to (B) a structural nucleic acid molecule, wherein the structural nucleic acid molecule is selected from the group consisting of a nucleic acid molecule that encodes a maize or soybean ribulose-bisphosphate carboxylase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean phosphoglycerate kinase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean glyceraldehyde 3-phosphate dehydrogenase enzyme or fragment thereof, a nucleic acid molecule that encodes a putative maize glyceraldehyde 3-phosphate dehydrogenase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean triose phosphate isomerase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean aldolase enzyme or fragments thereof, a nucleic acid molecule that encodes a maize or soybean fructose-1,6-bisphosphatase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean transketolase enzyme or fragments thereof, a nucleic acid molecule that encodes a putative maize or soybean transketolase enzyme or fragments thereof, a nucleic acid molecule that encodes a maize or soybean sedoheptulose-1,7-bisphosphatase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean D-ribulose-5-phosphate-3-epimerase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean ribose-5-phosphate isomerase enzyme or fragment thereof, a nucleic acid molecule that encodes a putative maize or soybean ribose-5-phosphate isomerase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean ribose-5-phosphate kinase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean phosphoenolpyruvate carboxylase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean NADP-dependent malate dehydrogenase enzyme or fragments thereof, a nucleic acid molecule that encodes a maize or soybean aspartate aminotransferase enzyme or fragment thereof, a nucleic acid molecule that encodes a putative maize or soybean aspartate aminotransferase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean alanine aminotransferase enzyme or fragments thereof, a nucleic acid molecule that encodes a maize or soybean NADP-dependent malic enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean NAD-dependent malic enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean PEP carboxykinase enzyme or fragment thereof, a nucleic acid molecule that encodes a putative soybean PEP carboxykinase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean pyruvate, phosphate dikinase enzyme or fragment thereof, and a nucleic acid molecule that encodes a maize or soybean pyrophosphatase enzyme or fragments thereof; which is linked to (C) a 3′ non-translated sequence that functions in the plant cell to cause termination of transcription and addition of polyadenylated ribonucleotides to a 3′ end of the mRNA molecule.

The present invention also provides a transformed plant having a nucleic acid molecule which comprises: (A) an exogenous promoter region which functions in a plant cell to cause the production of a mRNA molecule; which is linked to (B) a transcribed nucleic acid molecule with a transcribed strand and a non-transcribed strand, wherein the transcribed strand is complementary to a nucleic acid molecule comprising a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341 or fragment thereof; which is linked to (C) a 3′ non-translated sequence that functions in plant cells to cause termination of transcription and addition of polyadenylated ribonucleotides to a 3′ end of the mRNA molecule.

The present invention also provides a transformed plant having a nucleic acid molecule which comprises: (A) an exogenous promoter region which functions in a plant cell to cause the production of a mRNA molecule; which is linked to: (B) a transcribed nucleic acid molecule with a transcribed strand and a non-transcribed strand, wherein a transcribed mRNA of the transcribed strand is complementary to an endogenous mRNA molecule having a nucleic acid sequence selected from the group consisting of an endogenous mRNA molecule that encodes a maize or soybean ribulose-bisphosphate carboxylase enzyme or fragment thereof; an endogenous mRNA molecule that encodes a maize or soybean phosphoglycerate kinase enzyme or fragment thereof; an endogenous mRNA molecule that encodes a maize or soybean glyceraldehyde 3-phosphate dehydrogenase enzyme or fragment thereof; an endogenous mRNA molecule that encodes a putative maize glyceraldehyde 3-phosphate dehydrogenase enzyme or fragment thereof; an endogenous mRNA molecule that encodes a maize or soybean triose phosphate isomerase enzyme or fragment thereof; an endogenous mRNA molecule that encodes a maize or soybean aldolase enzyme or fragment thereof; an endogenous mRNA molecule that encodes a maize or soybean fructose-1,6-bisphosphatase enzyme or fragment thereof; an endogenous mRNA molecule that encodes a maize or soybean transketolase enzyme or fragment thereof; an endogenous mRNA molecule that encodes a putative maize or soybean transketolase enzyme or fragment thereof; an endogenous mRNA molecule that encodes a maize or soybean sedoheptulose-1,7-bisphosphatase enzyme or fragment thereof; an endogenous mRNA molecule that encodes a maize or soybean D-ribulose-5-phosphate-3-epimerase enzyme or fragment thereof; an endogenous mRNA molecule that encodes a maize or soybean ribose-5-phosphate isomerase enzyme or fragment thereof; an endogenous mRNA molecule that encodes a putative maize or soybean ribose-5-phosphate isomerase enzyme or fragment thereof; an endogenous mRNA molecule that encodes a maize or soybean ribose-5-phosphate kinase enzyme or fragment thereof; an endogenous mRNA molecule that encodes a maize or soybean phosphoenolpyruvate carboxylase enzyme or fragment thereof; an endogenous mRNA molecule that encodes a maize or soybean NADP-dependent malate dehydrogenase enzyme or fragment thereof; an endogenous mRNA molecule that encodes a maize or soybean aspartate aminotransferase enzyme or fragment thereof; an endogenous mRNA molecule that encodes a putative maize or soybean aspartate aminotransferase enzyme or fragment thereof; an endogenous mRNA molecule that encodes a maize or soybean alanine aminotransferase enzyme or fragment thereof; an endogenous mRNA molecule that encodes a maize or soybean NADP-dependent malic enzyme or fragment thereof; an endogenous mRNA molecule that encodes a maize or soybean NAD-dependent malic enzyme or fragment thereof; an endogenous mRNA molecule that encodes a maize or soybean PEP carboxykinase enzyme or fragment thereof; an endogenous mRNA molecule that encodes a putative soybean PEP carboxykinase enzyme or fragment thereof; an endogenous mRNA molecule that encodes a maize or soybean pyruvate, phosphate dikinase enzyme or fragment thereof; and an endogenous mRNA molecule that encodes a maize or soybean pyrophosphatase enzyme or fragment thereof; which is linked to (C) a 3′ non-translated sequence that functions in the plant cell to cause termination of transcription and addition of polyadenylated ribonucleotides to a 3′ end of the mRNA molecule.

The present invention also provides a method for determining a level or pattern of a plant carbon assimilation pathway enzyme in a plant cell or plant tissue comprising: (A) incubating, under conditions permitting nucleic acid hybridization, a marker nucleic acid molecule, the marker nucleic acid molecule having a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341 or complements thereof or fragment of either, with a complementary nucleic acid molecule obtained from the plant cell or plant tissue, wherein nucleic acid hybridization between the marker nucleic acid molecule and the complementary nucleic acid molecule obtained from the plant cell or plant tissue permits the detection of the plant carbon assimilation pathway enzyme; (B) permitting hybridization between the marker nucleic acid molecule and the complementary nucleic acid molecule obtained from the plant cell or plant tissue; and (C) detecting the level or pattern of the complementary nucleic acid, wherein the detection of the complementary nucleic acid is predictive of the level or pattern of the plant carbon assimilation pathway enzyme.

The present invention also provides a method for determining a level or pattern of a plant carbon assimilation pathway enzyme in a plant cell or plant tissue comprising: (A) incubating, under conditions permitting nucleic acid hybridization, a marker nucleic acid molecule, the marker nucleic acid molecule comprising a nucleic acid molecule that encodes a maize or soybean ribulose-bisphosphate carboxylase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean phosphoglycerate kinase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean glyceraldehyde 3-phosphate dehydrogenase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a putative maize glyceraldehyde 3-phosphate dehydrogenase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean triose phosphate isomerase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean aldolase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean fructose-1,6-bisphosphatase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean transketolase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a putative maize or soybean transketolase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean sedoheptulose-1,7-bisphosphatase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean D-ribulose-5-phosphate-3-epimerase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean ribose-5-phosphate isomerase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a putative maize or soybean ribose-5-phosphate isomerase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean ribose-5-phosphate kinase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean phosphoenolpyruvate carboxylase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean NADP-dependent malate dehydrogenase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean aspartate aminotransferase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a putative maize or soybean aspartate aminotransferase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean alanine aminotransferase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean NADP-dependent malic enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean NAD-dependent malic enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean PEP carboxykinase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a putative soybean PEP carboxykinase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean pyruvate, phosphate dikinase enzyme or complement thereof or fragment of either and a nucleic acid molecule that encodes a maize or soybean pyrophosphatase enzyme or complement thereof or fragment of either, with a complementary nucleic acid molecule obtained from the plant cell or plant tissue, wherein nucleic acid hybridization between the marker nucleic acid molecule and the complementary nucleic acid molecule obtained from the plant cell or plant tissue permits the detection of the plant carbon assimilation pathway enzyme; (B) permitting hybridization between the marker nucleic acid molecule and the complementary nucleic acid molecule obtained from the plant cell or plant tissue; and (C) detecting the level or pattern of the complementary nucleic acid, wherein the detection of the complementary nucleic acid is predictive of the level or pattern of the plant carbon assimilation pathway enzyme.

The present invention also provides a method for determining a level or pattern of a plant carbon assimilation pathway enzyme in a plant cell or plant tissue under evaluation which comprises assaying the concentration of a molecule, whose concentration is dependent upon the expression of a gene, the gene specifically hybridizes to a nucleic acid molecule having a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341 or complements thereof, in comparison to the concentration of that molecule present in a reference plant cell or a reference plant tissue with a known level or pattern of the plant carbon assimilation pathway enzyme, wherein the assayed concentration of the molecule is compared to the assayed concentration of the molecule in the reference plant cell or reference plant tissue with the known level or pattern of the plant carbon assimilation pathway enzyme.

The present invention also provides a method for determining a level or pattern of a plant carbon assimilation pathway enzyme in a plant cell or plant tissue under evaluation which comprises assaying the concentration of a molecule, whose concentration is dependent upon the expression of a gene, the gene specifically hybridizes to a nucleic acid molecule selected from the group consisting of a nucleic acid molecule that encodes a maize or soybean ribulose-bisphosphate carboxylase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean phosphoglycerate kinase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean glyceraldehyde 3-phosphate dehydrogenase enzyme or complement thereof, a nucleic acid molecule that encodes a putative maize glyceraldehyde 3-phosphate dehydrogenase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean triose phosphate isomerase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean aldolase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean fructose-1,6-bisphosphatase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean transketolase enzyme or complement thereof, a nucleic acid molecule that encodes a putative maize or soybean transketolase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean sedoheptulose-1,7-bisphosphatase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean D-ribulose-5-phosphate-3-epimerase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean ribose-5-phosphate isomerase enzyme or complement thereof, a nucleic acid molecule that encodes a putative maize or soybean ribose-5-phosphate isomerase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean ribose-5-phosphate kinase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean phosphoenolpyruvate carboxylase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean NADP-dependent malate dehydrogenase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean aspartate aminotransferase enzyme or complement thereof, a nucleic acid molecule that encodes a putative maize or soybean aspartate aminotransferase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean alanine aminotransferase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean NADP-dependent malic enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean NAD-dependent malic enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean PEP carboxykinase enzyme or complement thereof, a nucleic acid molecule that encodes a putative soybean PEP carboxykinase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean pyruvate, phosphate dikinase enzyme or complement thereof and a nucleic acid molecule that encodes a maize or soybean pyrophosphatase enzyme or complement thereof, in comparison to the concentration of that molecule present in a reference plant cell or a reference plant tissue with a known level or pattern of the plant carbon assimilation pathway enzyme, wherein the assayed concentration of the molecule is compared to the assayed concentration of the molecule in the reference plant cell or the reference plant tissue with the known level or pattern of the plant carbon assimilation pathway enzyme.

The present invention provides a method of determining a mutation in a plant whose presence is predictive of a mutation affecting a level or pattern of a protein comprising the steps: (A) incubating, under conditions permitting nucleic acid hybridization, a marker nucleic acid, the marker nucleic acid selected from the group of marker nucleic acid molecules which specifically hybridize to a nucleic acid molecule having a nucleic acid sequence selected from the group of SEQ ID NO: 1 through SEQ ID NO: 7341 or complements thereof or fragment of either and a complementary nucleic acid molecule obtained from the plant, wherein nucleic acid hybridization between the marker nucleic acid molecule and the complementary nucleic acid molecule obtained from the plant permits the detection of a polymorphism whose presence is predictive of a mutation affecting the level or pattern of the protein in the plant; (B) permitting hybridization between the marker nucleic acid molecule and the complementary nucleic acid molecule obtained from the plant; and (C) detecting the presence of the polymorphism, wherein the detection of the polymorphism is predictive of the mutation.

The present invention also provides a method for determining a mutation in a plant whose presence is predictive of a mutation affecting the level or pattern of a plant carbon assimilation pathway enzyme comprising the steps: (A) incubating, under conditions permitting nucleic acid hybridization, a marker nucleic acid molecule, the marker nucleic acid molecule comprising a nucleic acid molecule that is linked to a gene, the gene specifically hybridizes to a nucleic acid molecule having a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341 or complements thereof and a complementary nucleic acid molecule obtained from the plant, wherein nucleic acid hybridization between the marker nucleic acid molecule and the complementary nucleic acid molecule obtained from the plant permits the detection of a polymorphism whose presence is predictive of a mutation affecting the level or pattern of the plant carbon assimilation pathway enzyme in the plant; (B) permitting hybridization between the marker nucleic acid molecule and the complementary nucleic acid molecule obtained from the plant; and (C) detecting the presence of the polymorphism, wherein the detection of the polymorphism is predictive of the mutation.

The present invention also provides a method for determining a mutation in a plant whose presence is predictive of a mutation affecting the level or pattern of a plant carbon assimilation pathway enzyme comprising the steps: (A) incubating, under conditions permitting nucleic acid hybridization, a marker nucleic acid molecule, the marker nucleic acid molecule comprising a nucleic acid molecule that is linked to a gene, the gene specifically hybridizes to a nucleic acid molecule selected from the group consisting of a nucleic acid molecule that encodes a maize or soybean ribulose-bisphosphate carboxylase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean phosphoglycerate kinase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean glyceraldehyde 3-phosphate dehydrogenase enzyme or complement thereof, a nucleic acid molecule that encodes a putative maize glyceraldehyde 3-phosphate dehydrogenase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean triose phosphate isomerase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean aldolase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean fructose-1,6-bisphosphatase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean transketolase enzyme or complement thereof, a nucleic acid molecule that encodes a putative maize or soybean transketolase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean sedoheptulose-1,7-bisphosphatase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean D-ribulose-5-phosphate-3-epimerase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean ribose-5-phosphate isomerase enzyme or complement thereof, a nucleic acid molecule that encodes a putative maize or soybean ribose-5-phosphate isomerase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean ribose-5-phosphate kinase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean phosphoenolpyruvate carboxylase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean NADP-dependent malate dehydrogenase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean aspartate aminotransferase enzyme or complement thereof, a nucleic acid molecule that encodes a putative maize or soybean aspartate aminotransferase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean alanine aminotransferase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean NADP-dependent malic enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean NAD-dependent malic enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean PEP carboxykinase enzyme or complement thereof, a nucleic acid molecule that encodes a putative soybean PEP carboxykinase enzyme or complement thereof, a nucleic acid molecule that encodes a maize or soybean pyruvate, phosphate dikinase enzyme or complement thereof and a nucleic acid molecule that encodes a maize or soybean pyrophosphatase enzyme or complement thereof, and a complementary nucleic acid molecule obtained from the plant, wherein nucleic acid hybridization between the marker nucleic acid molecule and the complementary nucleic acid molecule obtained from the plant permits the detection of a polymorphism whose presence is predictive of a mutation affecting the level or pattern of the plant carbon assimilation pathway enzyme in the plant; (B) permitting hybridization between the marker nucleic acid molecule and the complementary nucleic acid molecule obtained from the plant; and (C) detecting the presence of the polymorphism, wherein the detection of the polymorphism is predictive of the mutation.

The present invention also provides a method of producing a plant containing an overexpressed protein comprising: (A) transforming the plant with a functional nucleic acid molecule, wherein the functional nucleic acid molecule comprises a promoter region, wherein the promoter region is linked to a structural region, wherein the structural region has a nucleic acid sequence selected from group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341; wherein the structural region is linked to a 3′ non-translated sequence that functions in the plant to cause termination of transcription and addition of polyadenylated ribonucleotides to a 3′ end of a mRNA molecule; and wherein the functional nucleic acid molecule results in overexpression of the protein; and (B) growing the transformed plant.

The present invention also provides a method of producing a plant containing an overexpressed plant carbon assimilation pathway enzyme comprising: (A) transforming the plant with a functional nucleic acid molecule, wherein the functional nucleic acid molecule comprises a promoter region, wherein the promoter region is linked to a structural region, wherein the structural region comprises a nucleic acid molecule having a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341 or fragment thereof; wherein the structural region is linked to a 3′ non-translated sequence that functions in the plant to cause termination of transcription and addition of polyadenylated ribonucleotides to a 3′ end of a mRNA molecule; and wherein the functional nucleic acid molecule results in overexpression of the plant carbon assimilation pathway enzyme; and (B) growing the transformed plant.

The present invention also provides a method of producing a plant containing an overexpressed plant carbon assimilation pathway enzyme comprising: (A) transforming the plant with a functional nucleic acid molecule, wherein the functional nucleic acid molecule comprises a promoter region, wherein the promoter region is linked to a structural region, wherein the structural region comprises a nucleic acid molecule selected from the group consisting of a nucleic acid molecule that encodes a maize or soybean ribulose-bisphosphate carboxylase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean phosphoglycerate kinase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean glyceraldehyde 3-phosphate dehydrogenase enzyme or fragment thereof, a nucleic acid molecule that encodes a putative maize glyceraldehyde 3-phosphate dehydrogenase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean triose phosphate isomerase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean aldolase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean fructose-1,6-bisphosphatase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean transketolase enzyme or fragment thereof, a nucleic acid molecule that encodes a putative maize or soybean transketolase enzyme or fragment thereof a nucleic acid molecule that encodes a maize or soybean sedoheptulose-1,7-bisphosphatase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean D-ribulose-5-phosphate-3-epimerase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean ribose-5-phosphate isomerase enzyme or fragment thereof, a nucleic acid molecule that encodes a putative maize or soybean ribose-5-phosphate isomerase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean ribose-5-phosphate kinase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean phosphoenolpyruvate carboxylase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean NADP-dependent malate dehydrogenase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean aspartate aminotransferase enzyme or fragment thereof, a nucleic acid molecule that encodes a putative maize or soybean aspartate aminotransferase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean alanine aminotransferase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean NADP-dependent malic enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean NAD-dependent malic enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean PEP carboxykinase enzyme or fragment thereof, a nucleic acid molecule that encodes a putative soybean PEP carboxykinase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean pyruvate, phosphate dikinase enzyme or fragment thereof and a nucleic acid molecule that encodes a maize or soybean pyrophosphatase enzyme or fragment thereof; wherein the structural region is linked to a 3′ non-translated sequence that functions in the plant to cause termination of transcription and addition of polyadenylated ribonucleotides to a 3′ end of a mRNA molecule; and wherein the functional nucleic acid molecule results in overexpression of the plant carbon assimilation pathway enzyme; and (B) growing the transformed plant.

The present invention also provides a method of producing a plant containing reduced levels of a plant carbon assimilation pathway enzyme comprising: (A) transforming the plant with a functional nucleic acid molecule, wherein the functional nucleic acid molecule comprises a promoter region, wherein the promoter region is linked to a structural region, wherein the structural region comprises a nucleic acid molecule having a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341; wherein the structural region is linked to a 3′ non-translated sequence that functions in the plant to cause termination of transcription and addition of polyadenylated ribonucleotides to a 3′ end of a mRNA molecule; and wherein the functional nucleic acid molecule results in co-suppression of the plant carbon assimilation pathway enzyme; and (B) growing the transformed plant.

The present invention also provides a method of producing a plant containing reduced levels of a plant carbon assimilation pathway enzyme comprising: (A) transforming the plant with a functional nucleic acid molecule, wherein the functional nucleic acid molecule comprises a promoter region, wherein the promoter region is linked to a structural region, wherein the structural region comprises a nucleic acid molecule having a nucleic acid sequence selected from the group consisting of a nucleic acid molecule that encodes a maize or soybean ribulose-bisphosphate carboxylase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean phosphoglycerate kinase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean glyceraldehyde 3-phosphate dehydrogenase enzyme or fragment thereof, a nucleic acid molecule that encodes a putative maize glyceraldehyde 3-phosphate dehydrogenase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean triose phosphate isomerase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean aldolase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean fructose-1,6-bisphosphatase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean transketolase enzyme or fragment thereof, a nucleic acid molecule that encodes a putative maize or soybean transketolase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean sedoheptulose-1,7-bisphosphatase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean D-ribulose-5-phosphate-3-epimerase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean ribose-5-phosphate isomerase enzyme or fragment thereof, a nucleic acid molecule that encodes a putative maize or soybean ribose-5-phosphate isomerase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean ribose-5-phosphate kinase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean phosphoenolpyruvate carboxylase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean NADP-dependent malate dehydrogenase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean aspartate aminotransferase enzyme or fragment thereof, a nucleic acid molecule that encodes a putative maize or soybean aspartate aminotransferase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean alanine aminotransferase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean NADP-dependent malic enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean NAD-dependent malic enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean PEP carboxykinase enzyme or fragment thereof, a nucleic acid molecule that encodes a putative soybean PEP carboxykinase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean pyruvate, phosphate dikinase enzyme or fragment thereof and a nucleic acid molecule that encodes a maize or soybean pyrophosphatase enzyme or fragment thereof wherein the structural region is linked to a 3′ non-translated sequence that functions in the plant to cause termination of transcription and addition of polyadenylated ribonucleotides to a 3′ end of a mRNA molecule; and wherein the functional nucleic acid molecule results in co-suppression of the plant carbon assimilation pathway enzyme; and (B) growing the transformed plant.

The present invention also provides a method for reducing expression of a plant carbon assimilation pathway enzyme in a plant comprising: (A) transforming the plant with a nucleic acid molecule, the nucleic acid molecule having an exogenous promoter region which functions in a plant cell to cause the production of a mRNA molecule, wherein the exogenous promoter region is linked to a transcribed nucleic acid molecule having a transcribed strand and a non-transcribed strand, wherein the transcribed strand is complementary to a nucleic acid molecule having a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341 or complements thereof or fragments of either and the transcribed strand is complementary to an endogenous mRNA molecule; and wherein the transcribed nucleic acid molecule is linked to a 3′ non-translated sequence that functions in the plant cell to cause termination of transcription and addition of polyadenylated ribonucleotides to a 3′ end of a mRNA molecule; and (B) growing the transformed plant.

The present invention also provides a method for reducing expression of a plant carbon assimilation pathway enzyme in a plant comprising: (A) transforming the plant with a nucleic acid molecule, the nucleic acid molecule having an exogenous promoter region which functions in a plant cell to cause the production of a mRNA molecule, wherein the exogenous promoter region is linked to a transcribed nucleic acid molecule having a transcribed strand and a non-transcribed strand, wherein a transcribed mRNA of the transcribed strand is complementary to a nucleic acid molecule selected from the group consisting of an endogenous mRNA molecule that encodes a maize or soybean ribulose-bisphosphate carboxylase enzyme or fragment thereof, an endogenous mRNA molecule that encodes a maize or soybean phosphoglycerate kinase enzyme or fragment thereof, an endogenous mRNA molecule that encodes a maize or soybean glyceraldehyde 3-phosphate dehydrogenase enzyme or fragment thereof, an endogenous mRNA molecule that encodes a putative maize glyceraldehyde 3-phosphate dehydrogenase enzyme or fragment thereof an endogenous mRNA molecule that encodes a maize or soybean triose phosphate isomerase enzyme or fragment thereof, an endogenous mRNA molecule that encodes a maize or soybean aldolase enzyme or fragment thereof, an endogenous mRNA molecule that encodes a maize or soybean fructose-1,6-bisphosphatase enzyme or fragment thereof, an endogenous mRNA molecule that encodes a maize or soybean transketolase enzyme or fragment thereof, an endogenous mRNA molecule that encodes a putative maize or soybean transketolase enzyme or fragment thereof, an endogenous mRNA molecule that encodes a maize or soybean sedoheptulose-1,7-bisphosphatase enzyme or fragment thereof, an endogenous mRNA molecule that encodes a maize or soybean D-ribulose-5-phosphate-3-epimerase enzyme or fragment thereof, an endogenous mRNA molecule that encodes a maize or soybean ribose-5-phosphate isomerase enzyme or fragment thereof, an endogenous mRNA molecule that encodes a putative maize or soybean ribose-5-phosphate isomerase enzyme or fragment thereof, an endogenous mRNA molecule that encodes a maize or soybean ribose-5-phosphate kinase enzyme or fragment thereof, an endogenous mRNA molecule that encodes a maize or soybean phosphoenolpyruvate carboxylase enzyme or fragment thereof, an endogenous mRNA molecule that encodes a maize or soybean NADP-dependent malate dehydrogenase enzyme or fragment thereof, an endogenous mRNA molecule that encodes a maize or soybean aspartate aminotransferase enzyme or fragment thereof, an endogenous mRNA molecule that encodes a putative maize or soybean aspartate aminotransferase enzyme or fragment thereof, an endogenous mRNA molecule that encodes a maize or soybean alanine aminotransferase enzyme or fragment thereof, an endogenous mRNA molecule that encodes a maize or soybean NADP-dependent malic enzyme or fragment thereof, an endogenous mRNA molecule that encodes a maize or soybean NAD-dependent malic enzyme or fragment thereof, an endogenous mRNA molecule that encodes a maize or soybean PEP carboxykinase enzyme or fragment thereof, an endogenous mRNA molecule that encodes a putative soybean PEP carboxykinase enzyme or fragment thereof, an endogenous mRNA molecule that encodes a maize or soybean pyruvate, phosphate dikinase enzyme or fragment thereof and an endogenous mRNA molecule that encodes a maize or soybean pyrophosphatase enzyme or fragment thereof, and wherein the transcribed nucleic acid molecule is linked to a 3′ non-translated sequence that functions in the plant cell to cause termination of transcription and addition of polyadenylated ribonucleotides to a 3′ end of a mRNA molecule; and (B) growing the transformed plant.

The present invention also provides a method of determining an association between a polymorphism and a plant trait comprising: (A) hybridizing a nucleic acid molecule specific for the polymorphism to genetic material of a plant, wherein the nucleic acid molecule has a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341 or complements thereof or fragment of either; and (B) calculating the degree of association between the polymorphism and the plant trait.

The present invention also provides a method of determining an association between a polymorphism and a plant trait comprising: (A) hybridizing a nucleic acid molecule specific for the polymorphism to genetic material of a plant, wherein the nucleic acid molecule is selected from the group consisting of a nucleic acid molecule that encodes a maize or soybean ribulose-bisphosphate carboxylase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean phosphoglycerate kinase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean glyceraldehyde 3-phosphate dehydrogenase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a putative maize glyceraldehyde 3-phosphate dehydrogenase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean triose phosphate isomerase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean aldolase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean fructose-1,6-bisphosphatase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean transketolase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a putative maize or soybean transketolase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean sedoheptulose-1,7-bisphophatase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean D-ribulose-5-phosphate-3-epimerase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean ribose-5-phosphate isomerase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a putative maize or soybean ribose-5-phosphate isomerase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean ribose-5-phosphate kinase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean phosphoenolpyruvate carboxylase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean NADP-dependent malate dehydrogenase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean aspartate aminotransferase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a putative maize or soybean aspartate aminotransferase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean alanine aminotransferase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean NADP-dependent malic enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean NAD-dependent malic enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean PEP carboxykinase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a putative soybean PEP carboxykinase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean pyruvate, phosphate dikinase enzyme or complement thereof or fragment of either and a nucleic acid molecule that encodes a maize or soybean pyrophosphatase enzyme or complement thereof or fragment of either; and (B) calculating the degree of association between the polymorphism and the plant trait.

The present invention also provides a method of isolating a nucleic acid that encodes a plant carbon assimilation pathway enzyme or fragment thereof comprising: (A) incubating under conditions permitting nucleic acid hybridization, a first nucleic acid molecule comprising a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341 or complements thereof or fragment of either with a complementary second nucleic acid molecule obtained from a plant cell or plant tissue; (B) permitting hybridization between the first nucleic acid molecule and the second nucleic acid molecule obtained from the plant cell or plant tissue; and (C) isolating the second nucleic acid molecule.

The present invention also provides a method of isolating a nucleic acid molecule that encodes a plant carbon assimilation pathway enzyme or fragment thereof comprising: (A) incubating under conditions permitting nucleic acid hybridization, a first nucleic acid molecule selected from the group consisting of a nucleic acid molecule that encodes a maize or soybean ribulose-bisphosphate carboxylase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean phosphoglycerate kinase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean glyceraldehyde 3-phosphate dehydrogenase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a putative maize glyceraldehyde 3-phosphate dehydrogenase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean triose phosphate isomerase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean aldolase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean fructose-1,6-bisphosphatase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean transketolase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a putative maize or soybean transketolase enzyme or complement thereof or fragment of either a nucleic acid molecule that encodes a maize or soybean sedoheptulose-1,7-bisphophatase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean D-ribulose-5-phosphate-3-epimerase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean ribose-5-phosphate isomerase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a putative maize or soybean ribose-5-phosphate isomerase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean ribose-5-phosphate kinase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean phosphoenolpyruvate carboxylase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean NADP-dependent malate dehydrogenase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean aspartate aminotransferase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a putative maize or soybean aspartate aminotransferase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean alanine aminotransferase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean NADP-dependent malic enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean NAD-dependent malic enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean PEP carboxykinase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a putative soybean PEP carboxykinase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean pyruvate, phosphate dikinase enzyme or complement thereof or fragment of either and a nucleic acid molecule that encodes a maize or soybean pyrophosphatase enzyme or complement thereof or fragment of either; with a complementary second nucleic acid molecule obtained from a plant cell or plant tissue; (B) permitting hybridization between the plant carbon assimilation pathway enzyme nucleic acid molecule and the complementary nucleic acid molecule obtained from the plant cell or plant tissue; and (C) isolating the second nucleic acid molecule.

DETAILED DESCRIPTION OF THE INVENTION Agents of the Present Invention Agents

(a) Nucleic Acid Molecules

Agents of the present invention include plant nucleic acid molecules and more preferably include maize and soybean nucleic acid molecules and more preferably include nucleic acid molecules of the maize genotypes B73 (Illinois Foundation Seeds, Champaign, Ill. U.S.A.), B73x Mo17 (Illinois Foundation Seeds, Champaign, Ill. U.S.A.), DK604 (Dekalb Genetics, Dekalb, Ill. U.S.A.), H99 (Illinois Foundation Seeds, Champaign, Ill. U.S.A.), RX601 (Asgrow Seed Company, Des Moines, Iowa), Mo17 (Illinois Foundation Seeds, Champaign, Ill. U.S.A.), and soybean types Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa), C1944 (United States Department of Agriculture (USDA) Soybean Germplasm Collection, Urbana, Ill. U.S.A.), Cristalina (USDA Soybean Germplasm Collection, Urbana, Ill. U.S.A.), FT108 (Monsoy, Brazil), Hartwig (USDA Soybean Germplasm Collection, Urbana, Ill. U.S.A.), BW211S Null (Tohoku University, Morioka, Japan), PI507354 (USDA Soybean Germplasm Collection, Urbana, Ill. U.S.A.), Asgrow A4922 (Asgrow Seed Company, Des Moines, Iowa U.S.A.), PI227687 (USDA Soybean Germplasm Collection, Urbana, Ill. U.S.A.), PI229358 (USDA Soybean Germplasm Collection, Urbana, Ill. U.S.A.) and Asgrow A3237 (Asgrow Seed Company, Des Moines, Iowa U.S.A.).

A subset of the nucleic acid molecules of the present invention includes nucleic acid molecules that are marker molecules. Another subset of the nucleic acid molecules of the present invention include nucleic acid molecules that encode a protein or fragment thereof. Another subset of the nucleic acid molecules of the present invention are EST molecules.

Fragment nucleic acid molecules may encode significant portion(s) of, or indeed most of, these nucleic acid molecules. Alternatively, the fragments may comprise smaller oligonucleotides (having from about 15 to about 250 nucleotide residues and more preferably, about 15 to about 30 nucleotide residues).

As used herein, an agent, be it a naturally occurring molecule or otherwise may be “substantially purified,” if desired, such that one or more molecules that is or may be present in a naturally occurring preparation containing that molecule will have been removed or will be present at a lower concentration than that at which it would normally be found.

The agents of the present invention will preferably be “biologically active” with respect to either a structural attribute, such as the capacity of a nucleic acid to hybridize to another nucleic acid molecule, or the ability of a protein to be bound by an antibody (or to compete with another molecule for such binding). Alternatively, such an attribute may be catalytic and thus involve the capacity of the agent to mediate a chemical reaction or response.

The agents of the present invention may also be recombinant. As used herein, the term recombinant means any agent (e.g. DNA, peptide etc.), that is, or results, however indirect, from human manipulation of a nucleic acid molecule.

It is understood that the agents of the present invention may be labeled with reagents that facilitate detection of the agent (e.g. fluorescent labels, Prober et al, Science 238:336-340 (1987); Albarella et al, EP 144914; chemical labels, Sheldon et al., U.S. Pat. No. 4,582,789; Albarella et al., U.S. Pat. No. 4,563,417; modified bases, Miyoshi et al., EP 119448, all of which are hereby incorporated by reference in their entirety).

It is further understood, that the present invention provides recombinant bacterial, mammalian, microbial, insect, fungal and plant cells and viral constructs comprising the agents of the present invention. (See, for example, Uses of the Agents of the Invention, Section (a) Plant Constructs and Plant Transformants; Section (b) Fungal Constructs and Fungal Transformants; Section (c) Mammalian Constructs and Transformed Mammalian Cells; Section (d) Insect Constructs and Transformed Insect Cells; and Section (e) Bacterial Constructs and Transformed Bacterial Cells)

Nucleic acid molecules or fragments thereof of the present invention are capable of specifically hybridizing to other nucleic acid molecules under certain circumstances. As used herein, two nucleic acid molecules are said to be capable of specifically hybridizing to one another if the two molecules are capable of forming an anti-parallel, double-stranded nucleic acid structure. A nucleic acid molecule is said to be the “complement” of another nucleic acid molecule if they exhibit complete complementarity. As used herein, molecules are said to exhibit “complete complementarity” when every nucleotide of one of the molecules is complementary to a nucleotide of the other. Two molecules are said to be “minimally complementary” if they can hybridize to one another with sufficient stability to permit them to remain annealed to one another under at least conventional “low-stringency” conditions. Similarly, the molecules are said to be “complementary” if they can hybridize to one another with sufficient stability to permit them to remain annealed to one another under conventional “high-stringency” conditions. Conventional stringency conditions are described by Sambrook et al., Molecular Cloning, A Laboratory Manual, 2nd Ed., Cold Spring Harbor Press, Cold Spring Harbor, N.Y. (1989) and by Haymes et al., Nucleic Acid Hybridization, A Practical Approach, IRL Press, Washington, D.C. (1985), the entirety of which is herein incorporated by reference. Departures from complete complementarity are therefore permissible, as long as such departures do not completely preclude the capacity of the molecules to form a double-stranded structure. Thus, in order for a nucleic acid molecule to serve as a primer or probe it need only be sufficiently complementary in sequence to be able to form a stable double-stranded structure under the particular solvent and salt concentrations employed.

Appropriate stringency conditions which promote DNA hybridization, for example, 6.0× sodium chloride/sodium citrate (SSC) at about 45° C., followed by awash of 2.0×SSC at 50° C., are known to those skilled in the art or can be found in Current Protocols in Molecular Biology, John Wiley & Sons, N.Y. (1989), 6.3.1-6.3.6. For example, the salt concentration in the wash step can be selected from a low stringency of about 2.0×SSC at 50° C. to a high stringency of about 0.2×SSC at 50° C. In addition, the temperature in the wash step can be increased from low stringency conditions at room temperature, about 22° C., to high stringency conditions at about 65° C. Both temperature and salt may be varied, or either the temperature or the salt concentration may be held constant while the other variable is changed.

In a preferred embodiment, a nucleic acid of the present invention will specifically hybridize to one or more of the nucleic acid molecules set forth in SEQ ID NO: 1 through SEQ ID NO: 7341 or complements thereof under moderately stringent conditions, for example at about 2.0×SSC and about 65° C.

In a particularly preferred embodiment, a nucleic acid of the present invention will include those nucleic acid molecules that specifically hybridize to one or more of the nucleic acid molecules set forth in SEQ ID NO: 1 through SEQ ID NO: 7341 or complements thereof under high stringency conditions such as 0.2×SSC and about 65° C.

In one aspect of the present invention, the nucleic acid molecules of the present invention have one or more of the nucleic acid sequences set forth in SEQ ID NO: 1 through SEQ ID NO: 7341 or complements thereof. In another aspect of the present invention, one or more of the nucleic acid molecules of the present invention share between 100% and 90% sequence identity with one or more of the nucleic acid sequences set forth in SEQ ID NO: 1 through SEQ ID NO: 7341 or complements thereof. In a further aspect of the present invention, one or more of the nucleic acid molecules of the present invention share between 100% and 95% sequence identity with one or more of the nucleic acid sequences set forth in SEQ ID NO: 1 through SEQ ID NO: 7341 or complements thereof. In a more preferred aspect of the present invention, one or more of the nucleic acid molecules of the present invention share between 100% and 98% sequence identity with one or more of the nucleic acid sequences set forth in SEQ ID NO: 1 through SEQ ID NO: 7341 or complements thereof. In an even more preferred aspect of the present invention, one or more of the nucleic acid molecules of the present invention share between 100% and 99% sequence identity with one or more of the sequences set forth in SEQ ID NO: 1 through SEQ ID NO: 7341 or complements thereof.

In a further more preferred aspect of the present invention, one or more of the nucleic acid molecules of the present invention exhibit 100% sequence identity with a nucleic acid molecule present within MONN01, SATMON001, SATMON003 through SATMON014, SATMON016, SATMON017, SATMON019 through SATMON031, SATMON033, SATMON034, SATMON˜001, SATMONN01, SATMONN04 through SATMONN06, CMz029 through CMz031, CMz033 through CMz037, CMz039 through CMz042, CMz044 through CMz045, CMz047 through CMz050, SOYMON001 through SOYMON038, Soy51 through Soy56, Soy58 through Soy62, Soy65 through Soy71, Soy 73 and Soy76 through Soy77 (Monsanto Company, St. Louis, Mo. U.S.A.).

(i) Nucleic Acid Molecules Encoding Proteins or Fragments Thereof

Nucleic acid molecules of the present invention can comprise sequences that encode a carbon assimilation pathway enzyme or fragment thereof. Such carbon assimilation pathway enzymes or fragments thereof include homologues of known carbon assimilation pathway enzymes in other organisms.

In a preferred embodiment of the present invention, a maize or soybean carbon assimilation pathway enzyme or fragment thereof of the present invention is a homologue of another plant carbon assimilation pathway enzyme. In another preferred embodiment of the present invention, a maize or soybean carbon assimilation pathway enzyme or fragment thereof of the present invention is a homologue of a fungal carbon assimilation pathway enzyme. In another preferred embodiment of the present invention, a maize or soybean carbon assimilation pathway enzyme or fragment thereof of the present invention is a homologue of a bacterial carbon assimilation pathway enzyme. In another preferred embodiment of the present invention, a soybean carbon assimilation pathway enzyme or fragment thereof of the present invention is a homologue of a maize carbon assimilation pathway enzyme. In another preferred embodiment of the present invention, a maize carbon assimilation pathway enzyme homologue or fragment thereof of the present invention is a homologue of a soybean carbon assimilation pathway enzyme. In another preferred embodiment of the present invention, a maize or soybean carbon assimilation pathway enzyme homologue or fragment thereof of the present invention is a homologue of an Arabidopsis thaliana carbon assimilation pathway enzyme.

In a preferred embodiment of the present invention, the nucleic molecule of the present invention encodes a maize or soybean carbon assimilation pathway enzyme or fragment thereof where a maize or soybean carbon assimilation pathway enzyme exhibits a BLAST probability score of greater than 1E-12, preferably a BLAST probability score of between about 1E-30 and about 1E-12, even more preferably a BLAST probability score of greater than 1E-30 with its homologue.

In another preferred embodiment of the present invention, the nucleic acid molecule encoding a maize or soybean carbon assimilation pathway enzyme or fragment thereof exhibits a % identity with its homologue of between about 25% and about 40%, more preferably of between about 40 and about 70%, even more preferably of between about 70% and about 90% and even more preferably between about 90% and 99%. In another preferred embodiment, of the present invention, a maize or soybean carbon assimilation pathway enzyme or fragments thereof exhibits a % identity with its homologue of 100%.

In a preferred embodiment of the present invention, the nucleic molecule of the present invention encodes a maize or soybean carbon assimilation pathway enzyme or fragment thereof where a maize or soybean carbon assimilation pathway enzyme exhibits a BLAST score of greater than 120, preferably a BLAST score of between about 1450 and about 120, even more preferably a BLAST score of greater than 1450 with its homologue.

Nucleic acid molecules of the present invention also include non-maize, non-soybean homologues. Preferred non-maize, non-soybean homologues are selected from the group consisting of alfalfa, Arabidopsis, barley, Brassica, broccoli, cabbage, citrus, cotton, garlic, oat, oilseed rape, onion, canola, flax, an ornamental plant, pea, peanut, pepper, potato, rice, rye, sorghum, strawberry, sugarcane, sugarbeet, tomato, wheat, poplar, pine, fir, eucalyptus, apple, lettuce, lentils, grape, banana, tea, turf grasses, sunflower, oil palm and Phaseolus.

In a preferred embodiment, nucleic acid molecules having SEQ ID NO: 1 through SEQ ID NO: 7341 or complements and fragments of either can be utilized to obtain such homologues.

The degeneracy of the genetic code, which allows different nucleic acid sequences to code for the same protein or peptide, is known in the literature. (U.S. Pat. No. 4,757,006, the entirety of which is herein incorporated by reference).

In an aspect of the present invention, one or more of the nucleic acid molecules of the present invention differ in nucleic acid sequence from those encoding a maize or soybean carbon assimilation pathway enzyme or fragment thereof in SEQ ID NO: 1 through SEQ ID NO: 7341 due to the degeneracy in the genetic code in that they encode the same carbon assimilation pathway enzyme but differ in nucleic acid sequence.

In another further aspect of the present invention, one or more of the nucleic acid molecules of the present invention differ in nucleic acid sequence from those encoding a maize or soybean carbon assimilation pathway enzyme or fragment thereof in SEQ ID NO: 1 through SEQ ID NO: 7341 due to fact that the different nucleic acid sequence encodes a carbon assimilation pathway enzyme having one or more conservative amino acid residue. Examples of conservative substitutions are set forth in Table 1. It is understood that codons capable of coding for such conservative substitutions are known in the art.

TABLE 1 Original Residue Conservative Substitutions Ala Ser Arg Lys Asn Gln; His Asp Glu Cys Ser; Ala Gln Asn Glu Asp Gly Pro His Asn; Gln Ile Leu; Val Leu Ile; Val Lys Arg; Gln; Glu Met Leu; Ile Phe Met; Leu; Tyr Ser Thr Thr Ser Trp Tyr Tyr Trp; Phe Val Ile; Leu

In a further aspect of the present invention, one or more of the nucleic acid molecules of the present invention differ in nucleic acid sequence from those encoding a maize or soybean carbon assimilation pathway enzyme or fragment thereof set forth in SEQ ID NO: 1 through SEQ ID NO: 7341 or fragment thereof due to the fact that one or more codons encoding an amino acid has been substituted for a codon that encodes a nonessential substitution of the amino acid originally encoded.

Agents of the present invention include nucleic acid molecules that encode a maize or soybean carbon assimilation pathway enzyme or fragment thereof and particularly substantially purified nucleic acid molecules selected from the group consisting of a nucleic acid molecule that encodes a maize or soybean ribulose-bisphosphate carboxylase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean phosphoglycerate kinase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean glyceraldehyde 3-phosphate dehydrogenase enzyme or fragment thereof, a nucleic acid molecule that encodes a putative maize glyceraldehyde 3-phosphate dehydrogenase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean triose phosphate isomerase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean aldolase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean fructose-1,6-bisphosphatase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean transketolase enzyme or fragment thereof, a nucleic acid molecule that encodes a putative maize or soybean transketolase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean sedoheptulose-1,7-bisphosphatase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean D-ribulose-5-phosphate-3-epimerase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean ribose-5-phosphate isomerase enzyme or fragment thereof, a nucleic acid molecule that encodes a putative maize or soybean ribose-5-phosphate isomerase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean ribose-5-phosphate kinase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean phosphoenolpyruvate carboxylase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean NADP-dependent malate dehydrogenase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean aspartate aminotransferase enzyme or fragment thereof, a nucleic acid molecule that encodes a putative maize or soybean aspartate aminotransferase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean alanine aminotransferase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean NADP-dependent malic enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean NAD-dependent malic enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean PEP carboxykinase enzyme or fragment thereof, a nucleic acid molecule that encodes a putative soybean PEP carboxykinase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean pyruvate, phosphate dikinase enzyme or fragment thereof and a nucleic acid molecule that encodes a maize or soybean pyrophospatase enzyme or fragment thereof.

Non-limiting examples of such nucleic acid molecules of the present invention are nucleic acid molecules comprising: SEQ ID NO: 1 through SEQ ID NO: 7341 or fragment thereof that encode for a plant carbon assimilation pathway enzyme or fragment thereof, SEQ ID NO: 1 through SEQ ID NO: 281 and SEQ ID NO: 282 through SEQ ID NO: 847 or fragment thereof that encode for a ribulose-bisphosphate carboxylase enzyme or fragment thereof, SEQ ID NO: 848 through SEQ ID NO: 1090 and SEQ ID NO: 1091 through SEQ ID NO: 1307 or fragment thereof that encode for a phosphoglycerate kinase enzyme or fragment thereof, SEQ ID NO: 1308 through SEQ ID NO: 2383 and SEQ ID NO: 2397 through SEQ ID NO: 3450 or fragment thereof that encodes for a glyceraldehyde 3-phosphate dehydrogenase enzyme or fragment thereof, SEQ ID NO: 2384 through SEQ ID NO: 2396 or fragment thereof that encodes for a putative glyceraldehyde 3-phosphate dehydrogenase enzyme or fragment thereof, SEQ ID NO: 3541 through SEQ ID NO: 3746 and SEQ ID NO: 3747 through SEQ ID NO: 3918 or fragment thereof that encode for a triose phosphate isomerase enzyme or fragment thereof, SEQ ID NO: 3919 through SEQ ID NO: 3963 and SEQ ID NO: 3964 through SEQ ID NO: 4370 or fragment thereof that encode for an aldolase enzyme or fragment thereof, SEQ ID NO: 4371 through SEQ ID NO: 4421 and SEQ ID NO: 4422 through SEQ ID NO: 4475 or fragment thereof that encode for a fructose-1,6-bisphosphatase enzyme or fragment thereof, SEQ ID NO: 4476 through SEQ ID NO: 4513 and SEQ ID NO: 4525 through SEQ ID NO: 4605 or fragment thereof that encode for a transketolase enzyme or fragment thereof, SEQ ID NO: 4514 through SEQ ID NO: 4524 and SEQ ID NO: 4606 through SEQ ID NO: 4612 or fragment thereof that encode for a putative transketolase enzyme or fragment thereof, SEQ ID NO: 4613 through SEQ ID NO: 4614 and SEQ ID NO: 4615 through SEQ ID NO: 4677 or fragment thereof that encode for a sedoheptulose-1,7-bisphosphatase enzyme or fragment thereof, SEQ ID NO: 4678 through SEQ ID NO: 4723 and SEQ ID NO: 4724 through SEQ ID NO: 4762 or fragment thereof that encode for a ribulose-5-phosphate-3-epimerase enzyme or fragment thereof, SEQ ID NO: 4763 through SEQ ID NO: 4769 and SEQ ID NO: 4772 through SEQ ID NO: 4776 or fragment thereof that encodes for a D-ribose-5-phosphate isomerase enzyme or fragment thereof, SEQ ID NO: 4770 through SEQ ID NO: 4771 and SEQ ID NO: 4777 through SEQ ID NO: 4781 or fragment thereof that encodes for a putative ribose-5-phosphate isomerase enzyme or fragment thereof, SEQ ID NO: 4782 through SEQ ID NO: 4832 and SEQ ID NO: 4833 through SEQ ID NO: 4908 or fragment thereof that encode for a ribose-5-phosphate kinase enzyme or fragment thereof, SEQ ID NO: 4909 through SEQ ED NO: 5282 and SEQ ID NO: 5283 through SEQ ID NO: 5371 or fragment thereof that encode for a phosphoenolpyruvate carboxylase enzyme or fragment thereof, SEQ ID NO: 5372 through SEQ ID NO: 5419 and SEQ ID NO: 5420 through SEQ ID NO: 5423 or fragment thereof that encode for a NADP-dependent malate dehydrogenase enzyme or fragment thereof, SEQ ID NO: 5424 through SEQ ID NO: 5596 and SEQ ID NO: 5601 through SEQ ID NO: 5719 or fragment thereof that encode for an asparate aminotransferase enzyme or fragment thereof, SEQ ID NO: 5597 through SEQ ID NO: 5600 and SEQ ID NO: 5720 through SEQ ID NO: 5727 or fragment thereof that encode for a putative asparate aminotransferase enzyme or fragment thereof, SEQ ID NO: 5728 through SEQ ID NO: 5888 and SEQ ID NO: 5889 through SEQ ID NO: 6004 or fragment thereof that encode for an alanine aminotransferase enzyme or fragment thereof, SEQ ID NO: 6005 through SEQ ID NO: 6223 and SEQ ID NO: 6224 through SEQ ID NO: 6287 or fragment thereof that encode for a NADP-dependent malic enzyme or fragment thereof, SEQ ID NO: 6022 through SEQ ID NO: 6023, SEQ ID NO: 6288 through SEQ ID NO: 6290 and SEQ ID NO: 6291 through SEQ ID NO: 6293 or fragment thereof that encodes for a NAD-dependent malic enzyme or fragment thereof, SEQ ID NO: 6294 through SEQ ID NO: 6353 and SEQ ID NO: 6354 through SEQ ID NO: 6387 or fragment thereof that encode for a PEP carboxykinase enzyme or fragment thereof, SEQ ID NO: 6388 or fragment thereof that encode for a putative PEP carboxykinase enzyme or fragment thereof, SEQ ID NO: 6389 through SEQ ID NO: 6847 and SEQ ID NO: 6848 through SEQ ID NO: 6850 or fragment thereof that encode for a pyruvate, phosphate dikinase enzyme or fragment thereof, and SEQ ID NO: 6851 through SEQ ID NO: 7154 and SEQ ID NO: 7155 through SEQ ID NO: 7341 or fragment thereof that encode for a pyrophosphatase enzyme or fragment thereof.

A nucleic acid molecule of the present invention can also encode an homologue of a maize or soybean ribulose-bisphosphate carboxylase enzyme or fragment thereof, a maize or soybean phosphoglycerate kinase enzyme or fragment thereof, a maize or soybean glyceraldehyde 3-phosphate dehydrogenase enzyme or fragment thereof, a putative maize or soybean glyceraldehyde 3-phosphate dehydrogenase enzyme or fragment thereof, a maize or soybean triose phosphate isomerase enzyme or fragment thereof, a maize or soybean aldolase enzyme or fragment thereof, a maize or soybean fructose-1,6-bisphosphatase enzyme or fragment thereof, a maize or soybean transketolase enzyme or fragment thereof, a putative maize or soybean transketolase enzyme or fragment thereof, a maize or soybean sedoheptulose-1,7-bisphosphatase enzyme or fragment thereof, a maize or soybean D-ribulose-5-phosphate-3-epimerase enzyme or fragment thereof, a maize or soybean ribose-5-phosphate isomerase enzyme or fragment thereof, a putative maize or soybean ribose-5-phosphate isomerase enzyme or fragment thereof, a maize or soybean ribose-5-phosphate kinase enzyme or fragment thereof, a maize or soybean phosphoenolpyruvate carboxylase enzyme or fragment thereof, a maize or soybean NADP-dependent malate dehydrogenase enzyme or fragment thereof, a maize or soybean aspartate aminotransferase enzyme or fragment thereof, a putative maize or soybean aspartate aminotransferase enzyme or fragment thereof, a maize or soybean alanine aminotransferase enzyme or fragment thereof, a maize or soybean NADP-dependent malic enzyme or fragment thereof, a maize or soybean NAD-dependent malic enzyme or fragment thereof, a maize or soybean PEP carboxykinase enzyme or fragment thereof, a putative maize or soybean PEP carboxykinase enzyme or fragment thereof, a maize or soybean pyruvate, phosphate dikinase enzyme or fragment thereof or a maize soybean pyrophosphatase enzyme or fragment thereof. As used herein a homologue protein molecule or fragment thereof is a counterpart protein molecule or fragment thereof in a second species (e.g., maize ribulose-bisphosphate carboxylase is a homologue of Arabidopsis ribulose-bisphosphate carboxylase).

(ii) Nucleic Acid Molecule Markers and Probes

One aspect of the present invention concerns markers that include nucleic acid molecules SEQ ID NO: 1 through SEQ ID NO: 7341 or complements thereof or fragments of either that can act as markers or other nucleic acid molecules of the present invention that can act as markers. Genetic markers of the present invention include “dominant” or “codominant” markers “Codominant markers” reveal the presence of two or more alleles (two per diploid individual) at a locus. “Dominant markers” reveal the presence of only a single allele per locus. The presence of the dominant marker phenotype (e.g., a band of DNA) is an indication that one allele is present in either the homozygous or heterozygous condition. The absence of the dominant marker phenotype (e.g. absence of a DNA band) is merely evidence that “some other” undefined allele is present. In the case of populations where individuals are predominantly homozygous and loci are predominately dimorphic, dominant and codominant markers can be equally valuable. As populations become more heterozygous and multi-allelic, codominant markers often become more informative of the genotype than dominant markers. Marker molecules can be, for example, capable of detecting polymorphisms such as single nucleotide polymorphisms (SNPs).

SNPs are single base changes in genomic DNA sequence. They occur at greater frequency and are spaced with a greater uniformly throughout a genome than other reported forms of polymorphism. The greater frequency and uniformity of SNPs means that there is greater probability that such a polymorphism will be found near or in a genetic locus of interest than would be the case for other polymorphisms. SNPs are located in protein-coding regions and noncoding regions of a genome. Some of these SNPs may result in defective or variant protein expression (e.g., as a results of mutations or defective splicing). Analysis (genotyping) of characterized SNPs can require only a plus/minus assay rather than a lengthy measurement, permitting easier automation.

SNPs can be characterized using any of a variety of methods. Such methods include the direct or indirect sequencing of the site, the use of restriction enzymes (Botstein et al., Am. J. Hum. Genet. 32:314-331 (1980), the entirety of which is herein incorporated reference; Konieczny and Ausubel, Plant J. 4:403-410 (1993), the entirety of which is herein incorporated by reference), enzymatic and chemical mismatch assays (Myers et al., Nature 313:495-498 (1985), the entirety of which is herein incorporated by reference), allele-specific PCR (Newton et al., Nucl. Acids Res. 17:2503-2516 (1989), the entirety of which is herein incorporated by reference; Wu et al., Proc. Natl. Acad. Sci. (U.S.A.) 86:2757-2760 (1989), the entirety of which is herein incorporated by reference), ligase chain reaction (Barany, Proc. Natl. Acad. Sci. (U.S.A.) 88:189-193 (1991), the entirety of which is herein incorporated by reference), single-strand conformation polymorphism analysis (Labrune et al., Am. J. Hum. Genet. 48: 1115-1120 (1991), the entirety of which is herein incorporated by reference), primer-directed nucleotide incorporation assays (Kuppuswami et al., Proc. Natl. Acad. Sci. USA 88:1143-1147 (1991), the entirety of which is herein incorporated by reference), dideoxy fingerprinting (Sarkar et al., Genomics 13:441-443 (1992), the entirety of which is herein incorporated by reference), solid-phase ELISA-based oligonucleotide ligation assays (Nikiforov et al., Nucl. Acids Res. 22:4167-4175 (1994), the entirety of which is herein incorporated by reference), oligonucleotide fluorescence-quenching assays (Livak et al., PCR Methods Appl. 4:357-362 (1995), the entirety of which is herein incorporated by reference), 5′-nuclease allele-specific hybridization TaqMan assay (Livak et al., Nature Genet. 9:341-342 (1995), the entirety of which is herein incorporated by reference), template-directed dye-terminator incorporation (TDI) assay (Chen and Kwok, Nucl. Acids Res. 25:347-353 (1997), the entirety of which is herein incorporated by reference), allele-specific molecular beacon assay (Tyagi et al., Nature Biotech. 16: 49-53 (1998), the entirety of which is herein incorporated by reference), PinPoint assay (Haff and Smirnov, Genome Res. 7:378-388 (1997), the entirety of which is herein incorporated by reference) and dCAPS analysis (Neff et al., Plant J. 14:387-392 (1998), the entirety of which is herein incorporated by reference).

Additional markers, such as AFLP markers, RFLP markers and RAPD markers, can be utilized (Walton, Seed World 22-29 (July, 1993), the entirety of which is herein incorporated by reference; Burow and Blake, Molecular Dissection of Complex Traits, 13-29, Paterson (ed.), CRC Press, New York (1988), the entirety of which is herein incorporated by reference). DNA markers can be developed from nucleic acid molecules using restriction endonucleases, the PCR and/or DNA sequence information. RFLP markers result from single base changes or insertions/deletions. These codominant markers are highly abundant in plant genomes, have a medium level of polymorphism and are developed by a combination of restriction endonuclease digestion and Southern blotting hybridization. CAPS are similarly developed from restriction nuclease digestion but only of specific PCR products. These markers are also codominant, have a medium level of polymorphism and are highly abundant in the genome. The CAPS result from single base changes and insertions/deletions.

Another marker type, RAPDs, are developed from DNA amplification with random primers and result from single base changes and insertions/deletions in plant genomes. They are dominant markers with a medium level of polymorphisms and are highly abundant. AFLP markers require using the PCR on a subset of restriction fragments from extended adapter primers. These markers are both dominant and codominant are highly abundant in genomes and exhibit a medium level of polymorphism.

SSRs require DNA sequence information. These codominant markers result from repeat length changes, are highly polymorphic and do not exhibit as high a degree of abundance in the genome as CAPS, AFLPs and RAPDs SNPs also require DNA sequence information. These codominant markers result from single base substitutions. They are highly abundant and exhibit a medium of polymorphism (Rafalski et al., In: Nonmammalian Genomic Analysis, Birren and Lai (ed.), Academic Press, San Diego, Calif., pp. 75-134 (1996), the entirety of which is herein incorporated by reference). It is understood that a nucleic acid molecule of the present invention may be used as a marker.

A PCR probe is a nucleic acid molecule capable of initiating a polymerase activity while in a double-stranded structure to with another nucleic acid. Various methods for determining the structure of PCR probes and PCR techniques exist in the art. Computer generated searches using programs such as Primer3 (www-genome.wi.mit.edu/cgi-bin/primer/primer3.cgi), STSPipeline (www-genome.wi.mit.edu/cgi-bin/www-STS_Pipeline), or GeneUp (Pesole et al., BioTechniques 25:112-123 (1998) the entirety of which is herein incorporated by reference), for example, can be used to identify potential PCR primers.

It is understood that a fragment of one or more of the nucleic acid molecules of the present invention may be a probe and specifically a PCR probe.

(b) Protein and Peptide Molecules

A class of agents comprises one or more of the protein or fragments thereof or peptide molecules encoded by SEQ ID NO: 1 through SEQ ID NO: 7341 or one or more of the protein or fragment thereof and peptide molecules encoded by other nucleic acid agents of the present invention. As used herein, the term “protein molecule” or “peptide molecule” includes any molecule that comprises five or more amino acids. It is well known in the art that proteins may undergo modification, including post-translational modifications, such as, but not limited to, disulfide bond formation, glycosylation, phosphorylation, or oligomerization. Thus, as used herein, the term “protein molecule” or “peptide molecule” includes any protein molecule that is modified by any biological or non-biological process. The terms “amino acid” and “amino acids” refer to all naturally occurring L-amino acids. This definition is meant to include norleucine, ornithine, homocysteine and homoserine.

Non-limiting examples of the protein or fragment thereof of the present invention include a maize or soybean carbon assimilation pathway enzyme or fragment thereof; a maize or soybean ribulose-bisphosphate carboxylase enzyme or fragment thereof, a maize or soybean phosphoglycerate kinase enzyme or fragment thereof, a maize or soybean glyceraldehyde 3-phosphate dehydrogenase enzyme or fragment thereof, a putative maize glyceraldehyde 3-phosphate dehydrogenase enzyme or fragment thereof, a maize or soybean triose phosphate isomerase enzyme or fragment thereof, a maize or soybean aldolase enzyme or fragment thereof, a maize or soybean fructose-1,6-bisphosphatase enzyme or fragment thereof, a maize or soybean transketolase enzyme or fragment thereof, a putative maize or soybean transketolase enzyme or fragment thereof, a maize or soybean sedoheptulose-1,7-bisphosphatase enzyme or fragment thereof, a maize or soybean D-ribulose-5-phosphate-3-epimerase enzyme or fragment thereof, a maize or soybean ribose-5-phosphate isomerase enzyme or fragment thereof, a putative maize or soybean ribose-5-phosphate isomerase enzyme or fragment thereof, a maize or soybean ribose-5-phosphate kinase enzyme or fragment thereof, a maize or soybean phosphoenolpyruvate carboxylase enzyme or fragment thereof, a maize or soybean NADP-dependent malate dehydrogenase enzyme or fragment thereof, a maize or soybean aspartate aminotransferase enzyme or fragment thereof, a maize or soybean alanine aminotransferase enzyme or fragment thereof, a maize or soybean NADP-dependent malic enzyme or fragment thereof, a maize or soybean NAD-dependent malic enzyme or fragment thereof, a maize or soybean PEP carboxykinase enzyme or fragment thereof, a putative soybean PEP carboxykinase enzyme or fragment thereof, a maize or soybean pyruvate, phosphate dikinase enzyme or fragment thereof, or a maize or soybean pyrophosphatase enzyme or fragment thereof.

Non-limiting examples of the protein or fragment molecules of the present invention are a carbon assimilation pathway enzyme or fragment thereof encoded by: SEQ ID NO: 1 through SEQ ID NO: 7341 or fragment thereof that encode for a carbon assimilation pathway enzyme or fragment thereof, SEQ ID NO: 1 through SEQ ID NO: 281 and SEQ ID NO: 282 through SEQ ID NO: 847 or fragment thereof that encode for a ribulose-bisphosphate carboxylase enzyme or fragment thereof, SEQ ID NO: 848 through SEQ ID NO: 1090 and SEQ ID NO: 1091 through SEQ ID NO: 1307 or fragment thereof that encode for a phosphoglycerate kinase enzyme or fragment thereof, SEQ ID NO: 1308 through SEQ ID NO: 2383 and SEQ ID NO: 2384 through SEQ ID NO: 3540 or fragment thereof that encodes for a glyceraldehyde 3-phosphate dehydrogenase enzyme or fragment thereof, SEQ ID NO: 2384 through SEQ ID NO: 2396 or fragment thereof that encodes for a putative glyceraldehyde 3-phosphate dehydrogenase enzyme or fragment thereof, SEQ ID NO: 3541 through SEQ ID NO: 3746 and SEQ ID NO: 3747 through SEQ ID NO: 3918 or fragment thereof that encode for a triose phosphate isomerase enzyme or fragment thereof, SEQ ID NO: 3919 through SEQ ID NO: 3963 and SEQ ID NO: 3964 through SEQ ID NO: 4370 or fragment thereof that encode for an aldolase enzyme or fragment thereof, SEQ ID NO: 4371 through SEQ ID NO: 4421 and SEQ ID NO: 4422 through SEQ ID NO: 4475 or fragment thereof that encode for a fructose-1,6-bisphosphatase enzyme or fragment thereof, SEQ ID NO: 4476 through SEQ ID NO: 4513 and SEQ ID NO: 4525 through SEQ ID NO: 4605 or fragment thereof that encode for a transketolase enzyme or fragment thereof, SEQ ID NO: 4514 through SEQ ID NO: 4524 and SEQ ID NO: 4606 through SEQ ID NO: 4612 or fragment thereof that encode for a putative transketolase enzyme or fragment thereof, SEQ ID NO: 4613 through SEQ ID NO: 4614- and SEQ ID NO: 4615 through SEQ ID NO: 4677 or fragment thereof that encode for a sedoheptulose-1,7-bisphosphatase enzyme or fragment thereof, SEQ ID NO: 4678 through SEQ ID NO: 4723 and SEQ ID NO: 4724 through SEQ ID NO: 4762 or fragment thereof that encode for a D-ribulose-5-phosphate-3-epimerase enzyme or fragment thereof, SEQ ID NO: 4763 through SEQ ID NO: 4769 and SEQ ID NO: 4772 through SEQ ID NO: 4776 or fragment thereof that encodes for a ribose-5-phosphate isomerase enzyme or fragment thereof, SEQ ID NO: 4770 through SEQ ID NO: 4771 and SEQ ID NO: 4777 through SEQ ID NO: 4781 or fragment thereof that encodes for a putative ribose-5-phosphate isomerase enzyme or fragment thereof, SEQ ID NO: 4782 through SEQ ID NO: 4832 and SEQ ID NO: 4833 through SEQ ID NO: 4908 or fragment thereof that encode for a ribose-5-phosphate kinase enzyme or fragment thereof, SEQ ID NO: 4909 through SEQ ID NO: 5282 and SEQ ID NO: 5283 through SEQ ID NO: 5371 or fragment thereof that encode for a phosphoenolpyruvate carboxylase enzyme or fragment thereof, SEQ ID NO: 5372 through SEQ ID NO: 5419 and SEQ ID NO: 5420 through SEQ ID NO: 5423 or fragment thereof that encode for a NADP-dependent malate dehydrogenase enzyme or fragment thereof, SEQ ID NO: 5424 through SEQ ID NO: 5596 and SEQ ID NO: 5601 through SEQ ID NO: 5719 or fragment thereof that encode for an asparate aminotransferase enzyme or fragment thereof, SEQ ID NO: 5597 through SEQ ID NO: 5600 and SEQ ID NO: 5720 through SEQ ID NO: 5727 or fragment thereof that encode for a putative asparate aminotransferase enzyme or fragment thereof, SEQ ID NO: 5728 through SEQ ID NO: 5888 and SEQ ID NO: 5889 through SEQ ID NO: 6004 or fragment thereof that encode for an alanine aminotransferase enzyme or fragment thereof, SEQ ID NO: 6005 through SEQ ID NO: 6223 and SEQ ID NO: 6224 through SEQ ID NO: 6287 or fragment thereof that encode for a NADP-dependent malic enzyme or fragment thereof, SEQ ID NO: 6022 through SEQ ID NO: 6023, SEQ ID NO: 6288 through SEQ ID NO: 6290 and SEQ ID NO: 6291 through SEQ ID NO: 6293 or fragment thereof that encodes for a NAD-dependent malic enzyme or fragment thereof, SEQ ID NO: 6294 through SEQ ID NO: 6353 and SEQ ID NO: 6354 through SEQ ID NO: 6387 or fragment thereof that encode for a PEP carboxykinase enzyme or fragment thereof, SEQ ID NO: 6388 or fragment thereof that encode for a putative PEP carboxykinase enzyme or fragment thereof, SEQ ID NO: 6389 through SEQ ID NO: 6847 and SEQ ID NO: 6848 through SEQ ID NO: 6850 or fragment thereof that encode for a pyruvate, phosphate dikinase enzyme or fragment thereof, and SEQ ID NO: 6851 through SEQ ID NO: 7154 and SEQ ID NO: 7155 through SEQ ID NO: 7341 or fragment thereof that encode for a pyrophosphatase enzyme or fragment thereof.

One or more of the protein or fragment of peptide molecules may be produced via chemical synthesis, or more preferably, by expressing in a suitable bacterial or eucaryotic host. Suitable methods for expression are described by Sambrook et al., (In: Molecular Cloning, A Laboratory Manual, 2nd Edition, Cold Spring Harbor Press, Cold Spring Harbor, N.Y. (1989)), or similar texts. For example, the protein may be expressed in, for example, Uses of the Agents of the Invention, Section (a) Plant Constructs and Plant Transformants; Section (b) Fungal Constructs and Fungal Transformants; Section (c) Mammalian Constructs and Transformed Mammalian Cells; Section (d) Insect Constructs and Transformed Insect Cells; and Section (e) Bacterial Constructs and Transformed Bacterial Cells.

A “protein fragment” is a peptide or polypeptide molecule whose amino acid sequence comprises a subset of the amino acid sequence of that protein. A protein or fragment thereof that comprises one or more additional peptide regions not derived from that protein is a “fusion” protein. Such molecules may be derivatized to contain carbohydrate or other moieties (such as keyhole limpet hemocyanin, etc.). Fusion protein or peptide molecules of the present invention are preferably produced via recombinant means.

Another class of agents comprise protein or peptide molecules or fragments or fusions thereof encoded by SEQ ID NO: 1 through SEQ ID NO: 7341 or complements thereof in which conservative, non-essential or non-relevant amino acid residues have been added, replaced or deleted. Computerized means for designing modifications in protein structure are known in the art (Dahiyat and Mayo, Science 278:82-87 (1997), the entirety of which is herein incorporated by reference).

The protein molecules of the present invention include plant homologue proteins. An example of such a homologue is a homologue protein of a non-maize or non-soybean plant species, that include but not limited to alfalfa, Arabidopsis, barley, Brassica, broccoli, cabbage, citrus, cotton, garlic, oat, oilseed rape, onion, canola, flax, an ornamental plant, pea, peanut, pepper, potato, rice, rye, sorghum, strawberry, sugarcane, sugarbeet, tomato, wheat, poplar, pine, fir, eucalyptus, apple, lettuce, lentils, grape, banana, tea, turf grasses, sunflower, oil palm, Phaseolus etc. Particularly preferred non-maize or non-soybean for use for the isolation of homologs would include, Arabidopsis, barley, cotton, oat, oilseed rape, rice, canola, ornamentals, sugarcane, sugarbeet, tomato, potato, wheat and turf grasses. Such a homologue can be obtained by any of a variety of methods. Most preferably, as indicated above, one or more of the disclosed sequences (SEQ ID NO: 1 through SEQ ID NO: 7341 or complements thereof) will be used to define a pair of primers that may be used to isolate the homologue-encoding nucleic acid molecules from any desired species. Such molecules can be expressed to yield homologues by recombinant means.

(c) Antibodies

One aspect of the present invention concerns antibodies, single-chain antigen binding molecules, or other proteins that specifically bind to one or more of the protein or peptide molecules of the present invention and their homologues, fusions or fragments. Such antibodies may be used to quantitatively or qualitatively detect the protein or peptide molecules of the present invention. As used herein, an antibody or peptide is said to “specifically bind” to a protein or peptide molecule of the present invention if such binding is not competitively inhibited by the presence of non-related molecules.

Nucleic acid molecules that encode all or part of the protein of the present invention can be expressed, via recombinant means, to yield protein or peptides that can in turn be used to elicit antibodies that are capable of binding the expressed protein or peptide. Such antibodies may be used in immunoassays for that protein. Such protein-encoding molecules, or their fragments may be a “fusion” molecule (i.e., a part of a larger nucleic acid molecule) such that, upon expression, a fusion protein is produced. It is understood that any of the nucleic acid molecules of the present invention may be expressed, via recombinant means, to yield proteins or peptides encoded by these nucleic acid molecules.

The antibodies that specifically bind proteins and protein fragments of the present invention may be polyclonal or monoclonal and may comprise intact immunoglobulins, or antigen binding portions of immunoglobulins fragments (such as (F(ab′), F(ab′)₂), or single-chain immunoglobulins producible, for example, via recombinant means. It is understood that practitioners are familiar with the standard resource materials which describe specific conditions and procedures for the construction, manipulation and isolation of antibodies (see, for example, Harlow and Lane, In: Antibodies: A Laboratory Manual, Cold Spring Harbor Press, Cold Spring Harbor, N.Y. (1988), the entirety of which is herein incorporated by reference).

Murine monoclonal antibodies are particularly preferred. BALB/c mice are preferred for this purpose, however, equivalent strains may also be used. The animals are preferably immunized with approximately 25 μg of purified protein (or fragment thereof) that has been emulsified in a suitable adjuvant (such as TiterMax adjuvant (Vaxcel, Norcross, Ga.)). Immunization is preferably conducted at two intramuscular sites, one intraperitoneal site and one subcutaneous site at the base of the tail. An additional i.v. injection of approximately 25 μg of antigen is preferably given in normal saline three weeks later. After approximately 11 days following the second injection, the mice may be bled and the blood screened for the presence of anti-protein or peptide antibodies. Preferably, a direct binding Enzyme-Linked Immunoassay (ELISA) is employed for this purpose.

More preferably, the mouse having the highest antibody titer is given a third i.v. injection of approximately 25 μg of the same protein or fragment. The splenic leukocytes from this animal may be recovered 3 days later and then permitted to fuse, most preferably, using polyethylene glycol, with cells of a suitable myeloma cell line (such as, for example, the P3X63Ag8.653 myeloma cell line). Hybridoma cells are selected by culturing the cells under “HAT” (hypoxanthine-aminopterin-thymine) selection for about one week. The resulting clones may then be screened for their capacity to produce monoclonal antibodies (“mAbs”), preferably by direct ELISA.

In one embodiment, anti-protein or peptide monoclonal antibodies are isolated using a fusion of a protein or peptide of the present invention, or conjugate of a protein or peptide of the present invention, as immunogens. Thus, for example, a group of mice can be immunized using a fusion protein emulsified in Freund's complete adjuvant (e.g. approximately 50 μg of antigen per immunization). At three week intervals, an identical amount of antigen is emulsified in Freund's incomplete adjuvant and used to immunize the animals. Ten days following the third immunization, serum samples are taken and evaluated for the presence of antibody. If antibody titers are too low, a fourth booster can be employed. Polysera capable of binding the protein or peptide can also be obtained using this method.

In a preferred procedure for obtaining monoclonal antibodies, the spleens of the above-described immunized mice are removed, disrupted and immune splenocytes are isolated over a ficoll gradient. The isolated splenocytes are fused, using polyethylene glycol with BALB/c-derived HGPRT (hypoxanthine guanine phosphoribosyl transferase) deficient P3x63xAg8.653 plasmacytoma cells. The fused cells are plated into 96 well microtiter plates and screened for hybridoma fusion cells by their capacity to grow in culture medium supplemented with hypothanthine, aminopterin and thymidine for approximately 2-3 weeks.

Hybridoma cells that arise from such incubation are preferably screened for their capacity to produce an immunoglobulin that binds to a protein of interest. An indirect ELISA may be used for this purpose. In brief, the supernatants of hybridomas are incubated in microtiter wells that contain immobilized protein. After washing, the titer of bound immunoglobulin can be determined using, for example, a goat anti-mouse antibody conjugated to horseradish peroxidase. After additional washing, the amount of immobilized enzyme is determined (for example through the use of a chromogenic substrate). Such screening is performed as quickly as possible after the identification of the hybridoma in order to ensure that a desired clone is not overgrown by non-secreting neighbor cells. Desirably, the fusion plates are screened several times since the rates of hybridoma growth vary. In a preferred sub-embodiment, a different antigenic form may be used to screen the hybridoma. Thus, for example, the splenocytes may be immunized with one immunogen, but the resulting hybridomas can be screened using a different immunogen. It is understood that any of the protein or peptide molecules of the present invention may be used to raise antibodies.

As discussed below, such antibody molecules or their fragments may be used for diagnostic purposes. Where the antibodies are intended for diagnostic purposes, it may be desirable to derivatize them, for example with a ligand group (such as biotin) or a detectable marker group (such as a fluorescent group, a radioisotope or an enzyme).

The ability to produce antibodies that bind the protein or peptide molecules of the present invention permits the identification of mimetic compounds of those molecules. A “mimetic compound” is a compound that is not that compound, or a fragment of that compound, but which nonetheless exhibits an ability to specifically bind to antibodies directed against that compound.

It is understood that any of the agents of the present invention can be substantially purified and/or be biologically active and/or recombinant.

Uses of the Agents of the Invention

Nucleic acid molecules and fragments thereof of the present invention may be employed to obtain other nucleic acid molecules from the same species (e.g., ESTs or fragment thereof from maize may be utilized to obtain other nucleic acid molecules from maize). Such nucleic acid molecules include the nucleic acid molecules that encode the complete coding sequence of a protein and promoters and flanking sequences of such molecules. In addition, such nucleic acid molecules include nucleic acid molecules that encode for other isozymes or gene family members. Such molecules can be readily obtained by using the above-described nucleic acid molecules or fragments thereof to screen cDNA or genomic libraries obtained from maize or soybean. Methods for forming such libraries are well known in the art.

Nucleic acid molecules and fragments thereof of the present invention may also be employed to obtain nucleic acid homologues. Such homologues include the nucleic acid molecule of other plants or other organisms (e.g., alfalfa, Arabidopsis, barley, Brassica, broccoli, cabbage, citrus, cotton, garlic, oat, oilseed rape, onion, canola, flax, an ornamental plant, pea, peanut, pepper, potato, rice, rye, sorghum, strawberry, sugarcane, sugarbeet, tomato, wheat, poplar, pine, fir, eucalyptus, apple, lettuce, lentils, grape, banana, tea, turf grasses, sunflower, oil palm, Phaseolus, etc.) including the nucleic acid molecules that encode, in whole or in part, protein homologues of other plant species or other organisms, sequences of genetic elements such as promoters and transcriptional regulatory elements. Such molecules can be readily obtained by using the above-described nucleic acid molecules or fragments thereof to screen cDNA or genomic libraries obtained from such plant species. Methods for forming such libraries are well known in the art. Such homologue molecules may differ in their nucleotide sequences from those found in one or more of SEQ ID NO: 1 through SEQ. ID NO: 7341 or complements thereof because complete complementarity is not needed for stable hybridization. The nucleic acid molecules of the present invention therefore also include molecules that, although capable of specifically hybridizing with the nucleic acid molecules may lack “complete complementarity.”

Any of a variety of methods may be used to obtain one or more of the above-described nucleic acid molecules (Zarnechik et al., Proc. Natl. Acad. Sci. (U.S.A.) 83:4143-4146 (1986), the entirety of which is herein incorporated by reference; Goodchild et al., Proc. Natl. Acad. Sci. (U.S.A.) 85:5507-5511 (1988), the entirety of which is herein incorporated by reference; Wickstrom et al., Proc. Natl. Acad. Sci. (U.S.A.) 85:1028-1032 (1988), the entirety of which, is herein incorporated by reference; Holt et al., Molec. Cell. Biol. 8:963-973 (1988), the entirety of which is herein incorporated by reference; Gerwirtz et al., Science 242:1303-1306 (1988), the entirety of which is herein incorporated by reference; Anfossi et al., Proc. Natl. Acad. Sci. (U.S.A.) 86:3379-3383 (1989), the entirety of which is herein incorporated by reference; Becker et al., EMBO J. 8:3685-3691 (1989); the entirety of which is herein incorporated by reference). Automated nucleic acid synthesizers may be employed for this purpose. In lieu of such synthesis, the disclosed nucleic acid molecules may be used to define a pair of primers that can be used with the polymerase chain reaction (Mullis et al., Cold Spring Harbor Symp. Quant. Biol. 51:263-273 (1986); Erlich et al., European Patent 50,424; European Patent 84,796; European Patent 258,017; European Patent 237,362; Mullis, European Patent 201,184; Mullis et al., U.S. Pat. No. 4,683,202; Erlich, U.S. Pat. No. 4,582,788; and Saiki et al., U.S. Pat. No. 4,683,194, all of which are herein incorporated by reference in their entirety) to amplify and obtain any desired nucleic acid molecule or fragment.

Promoter sequence(s) and other genetic elements, including but not limited to transcriptional regulatory flanking sequences, associated with one or more of the disclosed nucleic acid sequences can also be obtained using the disclosed nucleic acid sequence provided herein. In one embodiment, such sequences are obtained by incubating EST nucleic acid molecules or preferably fragments thereof with members of genomic libraries (e.g. maize and soybean) and recovering clones that hybridize to the EST nucleic acid molecule or fragment thereof. In a second embodiment, methods of “chromosome walking,” or inverse PCR may be used to obtain such sequences (Frohman et al., Proc. Natl. Acad. Sci. (U.S.A.) 85:8998-9002 (1988); Ohara et al., Proc. Natl. Acad. Sci. (U.S.A.) 86:5673-5677 (1989); Pang et al., Biotechniques 22:1046-1048 (1977); Huang et al., Methods Mol. Biol. 69:89-96 (1997); Huang et al., Method Mol. Biol. 67:287-294 (1997); Benkel et al., Genet. Anal. 13:123-127 (1996); Hartl et al., Methods Mol. Biol. 58:293-301 (1996), all of which are herein incorporated by reference in their entirety).

The nucleic acid molecules of the present invention may be used to isolate promoters of cell enhanced, cell specific, tissue enhanced, tissue specific, developmentally or environmentally regulated expression profiles. Isolation and functional analysis of the 5′ flanking promoter sequences of these genes from genomic libraries, for example, using genomic screening methods and PCR techniques would result in the isolation of useful promoters and transcriptional regulatory elements. These methods are known to those of skill in the art and have been described (See, for example, Birren et al., Genome Analysis: Analyzing DNA, 1, (1997), Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., the entirety of which is herein incorporated by reference). Promoters obtained utilizing the nucleic acid molecules of the present invention could also be modified to affect their control characteristics. Examples of such modifications would include but are not limited to enhanced sequences as reported in Uses of the Agents of the Invention, Section (a) Plant Constructs and Plant Transformants. Such genetic elements could be used to enhance gene expression of new and existing traits for crop improvements.

In one sub-aspect, such an analysis is conducted by determining the presence and/or identity of polymorphism(s) by one or more of the nucleic acid molecules of the present invention and more preferably one or more of the EST nucleic acid molecule or fragment thereof which are associated with a phenotype, or a predisposition to that phenotype.

Any of a variety of molecules can be used to identify such polymorphism(s). In one embodiment, one or more of the EST nucleic acid molecules (or a sub-fragment thereof) may be employed as a marker nucleic acid molecule to identify such polymorphism(s). Alternatively, such polymorphisms can be detected through the use of a marker nucleic acid molecule or a marker protein that is genetically linked to (i.e., a polynucleotide that co-segregates with) such polymorphism(s).

In an alternative embodiment, such polymorphisms can be detected through the use of a marker nucleic acid molecule that is physically linked to such polymorphism(s). For this purpose, marker nucleic acid molecules comprising a nucleotide sequence of a polynucleotide located within 1 mb of the polymorphism(s) and more preferably within 100 kb of the polymorphism(s) and most preferably within 10 kb of the polymorphism(s) can be employed.

The genomes of animals and plants naturally undergo spontaneous mutation in the course of their continuing evolution (Gusella, Ann. Rev. Biochem. 55:831-854 (1986)). A “polymorphism” is a variation or difference in the sequence of the gene or its flanking regions that arises in some of the members of a species. The variant sequence and the “original” sequence co-exist in the species' population. In some instances, such co-existence is in stable or quasi-stable equilibrium.

A polymorphism is thus said to be “allelic,” in that, due to the existence of the polymorphism, some members of a species may have the original sequence (i.e., the original “allele”) whereas other members may have the variant sequence (i.e., the variant “allele”). In the simplest case, only one variant sequence may exist and the polymorphism is thus said to be di-allelic. In other cases, the species' population may contain multiple alleles and the polymorphism is termed tri-allelic, etc. A single gene may have multiple different unrelated polymorphisms. For example, it may have a di-allelic polymorphism at one site and a multi-allelic polymorphism at another site.

The variation that defines the polymorphism may range from a single nucleotide variation to the insertion or deletion of extended regions within a gene. In some cases, the DNA sequence variations are in regions of the genome that are characterized by short tandem repeats (STRs) that include tandem di- or tri-nucleotide repeated motifs of nucleotides. Polymorphisms characterized by such tandem repeats are referred to as “variable number tandem repeat” (“VNTR”) polymorphisms. VNTRs have been used in identity analysis (Weber, U.S. Pat. No. 5,075,217; Armour et al., FEBS Lett. 307:113-115 (1992); Jones et al., Eur. J. Haematol. 39:144-147 (1987); Horn et al., PCT Patent Application WO91/14003; Jeffreys, European Patent Application 370,719; Jeffreys, U.S. Pat. No. 5,175,082; Jeffreys et al., Amer. J. Hum. Genet. 39:11-24 (1986); Jeffreys et al., Nature 316:76-79 (1985); Gray et al., Proc. R. Acad. Soc. Lond. 243:241-253 (1991); Moore et al., Genomics 10:654-660 (1991); Jeffreys et al., Anim. Genet. 18:1-15 (1987); Hillel et al., Anim. Genet. 20:145-155 (1989); Hillel et al., Genet. 124:783-789 (1990), all of which are herein incorporated by reference in their entirety).

The detection of polymorphic sites in a sample of DNA may be facilitated through the use of nucleic acid amplification methods. Such methods specifically increase the concentration of polynucleotides that span the polymorphic site, or include that site and sequences located either distal or proximal to it. Such amplified molecules can be readily detected by gel electrophoresis or other means.

The most preferred method of achieving such amplification employs the polymerase chain reaction (“PCR”) (Mullis et al., Cold Spring Harbor Symp. Quant. Biol. 51:263-273 (1986); Erlich et al., European Patent Appln. 50,424; European Patent Appln. 84,796; European Patent Application 258,017; European Patent Appln. 237,362; Mullis, European Patent Appln. 201,184; Mullis et al., U.S. Pat. No. 4,683,202; Erlich, U.S. Pat. No. 4,582,788; and Saiki et al., U.S. Pat. No. 4,683,194), using primer pairs that are capable of hybridizing to the proximal sequences that define a polymorphism in its double-stranded form.

In lieu of PCR, alternative methods, such as the “Ligase Chain Reaction” (“LCR”) may be used (Barany, Proc. Natl. Acad. Sci. (U.S.A.) 88:189-193 (1991), the entirety of which is herein incorporated by reference). LCR uses two pairs of oligonucleotide probes to exponentially amplify a specific target. The sequences of each pair of oligonucleotides is selected to permit the pair to hybridize to abutting sequences of the same strand of the target. Such hybridization forms a substrate for a template-dependent ligase. As with PCR, the resulting products thus serve as a template in subsequent cycles and an exponential amplification of the desired sequence is obtained.

LCR can be performed with oligonucleotides having the proximal and distal sequences of the same strand of a polymorphic site. In one embodiment, either oligonucleotide will be designed to include the actual polymorphic site of the polymorphism. In such an embodiment, the reaction conditions are selected such that the oligonucleotides can be ligated together only if the target molecule either contains or lacks the specific nucleotide that is complementary to the polymorphic site present on the oligonucleotide. Alternatively, the oligonucleotides may be selected such that they do not include the polymorphic site (see, Segev, PCT Application WO 90/01069, the entirety of which is herein incorporated by reference).

The “Oligonucleotide Ligation Assay” (“OLA”) may alternatively be employed (Landegren et al., Science 241:1077-1080 (1988), the entirety of which is herein incorporated by reference). The OLA protocol uses two oligonucleotides which are designed to be capable of hybridizing to abutting sequences of a single strand of a target. OLA, like LCR, is particularly suited for the detection of point mutations. Unlike LCR, however, OLA results in “linear” rather than exponential amplification of the target sequence.

Nickerson et al., have described a nucleic acid detection assay that combines attributes of PCR and OLA (Nickerson et al., Proc. Natl. Acad. Sci. (U.S.A.) 87:8923-8927 (1990), the entirety of which is herein incorporated by reference). In this method, PCR is used to achieve the exponential amplification of target DNA, which is then detected using OLA. In addition to requiring multiple and separate, processing steps, one problem associated with such combinations is that they inherit all of the problems associated with PCR and OLA.

Schemes based on ligation of two (or more) oligonucleotides in the presence of nucleic acid having the sequence of the resulting “di-oligonucleotide”, thereby amplifying the di-oligonucleotide, are also known (Wu et al., Genomics 4:560-569 (1989), the entirety of which is herein incorporated by reference) and may be readily adapted to the purposes of the present invention.

Other known nucleic acid amplification procedures, such as allele-specific oligomers, branched DNA technology, transcription-based amplification systems, or isothermal amplification methods may also be used to amplify and analyze such polymorphisms (Malek et al., U.S. Pat. No. 5,130,238; Davey et al., European Patent Application 329,822; Schuster et al., U.S. Pat. No. 5,169,766; Miller et al., PCT Patent Application WO 89/06700; Kwoh et al., Proc. Natl. Acad. Sci. (U.S.A.) 86:1173-1177 (1989); Gingeras et al., PCT Patent Application WO 88/10315; Walker et al., Proc. Natl. Acad. Sci. (U.S.A.) 89:392-396 (1992), all of which are herein incorporated by reference in their entirety).

The identification of a polymorphism can be determined in a variety of ways. By correlating the presence or absence of it in a plant with the presence or absence of a phenotype, it is possible to predict the phenotype of that plant. If a polymorphism creates or destroys a restriction endonuclease cleavage site, or if it results in the loss or insertion of DNA (e.g., a VNTR polymorphism), it will alter the size or profile of the DNA fragments that are generated by digestion with that restriction endonuclease. As such, individuals that possess a variant sequence can be distinguished from those having the original sequence by restriction fragment analysis. Polymorphisms that can be identified in this manner are termed “restriction fragment length polymorphisms” (“RFLPs”). RFLPs have been widely used in human and plant genetic analyses (Glassberg, UK Patent Application 2135774; Skolnick et al., Cytogen. Cell Genet. 32:58-67 (1982); Botstein et al., Ann. J. Hum. Genet. 32:314-331 (1980); Fischer et al., (PCT Application WO90/13668); Uhlen, PCT Application WO90/11369).

Polymorphisms can also be identified by Single Strand Conformation Polymorphism (SSCP) analysis. SSCP is a method capable of identifying most sequence variations in a single strand of DNA, typically between 150 and 250 nucleotides in length (Elles, Methods in Molecular Medicine Molecular Diagnosis of Genetic Diseases, Humana Press (1996), the entirety of which is herein incorporated by reference); Orita et al., Genomics 5:874-879 (1989), the entirety of which is herein incorporated by reference). Under denaturing conditions a single strand of DNA will adopt a conformation that is uniquely dependent on its sequence conformation. This conformation usually will be different, even if only a single base is changed. Most conformations have been reported to alter the physical configuration or size sufficiently to be detectable by electrophoresis. A number of protocols have been described for SSCP including, but not limited to, Lee et al., Anal. Biochem. 205:289-293 (1992), the entirety of which is herein incorporated by reference; Suzuki et al., Anal. Biochem. 192:82-84 (1991), the entirety of which is herein incorporated by reference; Lo et al., Nucleic Acids Research 20:1005-1009 (1992), the entirety of which is herein incorporated by reference; Sarkar et al., Genomics 13:441-443 (1992), the entirety of which is herein incorporated by reference. It is understood that one or more of the nucleic acids of the present invention, may be utilized as markers or probes to detect polymorphisms by SSCP analysis.

Polymorphisms may also be found using a DNA fingerprinting technique called amplified fragment length polymorphism (AFLP), which is based on the selective PCR amplification of restriction fragments from a total digest of genomic DNA to profile that DNA (Vos et al., Nucleic Acids Res. 23:4407-4414 (1995), the entirety of which is herein incorporated by reference). This method allows for the specific co-amplification of high numbers of restriction fragments, which can be visualized by PCR without knowledge of the nucleic acid sequence.

AFLP employs basically three steps. Initially, a sample of genomic DNA is cut with restriction enzymes and oligonucleotide adapters are ligated to the restriction fragments of the DNA. The restriction fragments are then amplified using PCR by using the adapter and restriction sequence as target sites for primer annealing. The selective amplification is achieved by the use of primers that extend into the restriction fragments, amplifying only those fragments in which the primer extensions match the nucleotide flanking the restriction sites. These amplified fragments are then visualized on a denaturing polyacrylamide gel.

AFLP analysis has been performed on Salix (Beismann et al., Mol. Ecol. 6:989-993 (1997), the entirety of which is herein incorporated by reference), Acinetobacter (Janssen et al, Int. J. Syst. Bacteriol. 47:1179-1187 (1997), the entirety of which is herein incorporated by reference), Aeromonas popoffi (Huys et al, Int. J. Syst. Bacteriol. 47:1165-1171 (1997), the entirety of which is herein incorporated by reference), rice (McCouch et al, Plant Mol. Biol. 35:89-99 (1997), the entirety of which is herein incorporated by reference; Nandi et al., Mol. Gen. Genet. 255:1-8 (1997), the entirety of which is herein incorporated by reference; Cho et al., Genome 39:373-378 (1996), the entirety of which is herein incorporated by reference), barley (Hordeum vulgare) (Simons et al., Genomics 44:61-70 (1997), the entirety of which is herein incorporated by reference; Waugh et al., Mol. Gen. Genet. 255:311-321 (1997), the entirety of which is herein incorporated by reference; Qi et al, Mol. Gen. Genet. 254:330-336 (1997), the entirety of which is herein incorporated by reference; Becker et al., Mol. Gen. Genet. 249:65-73 (1995), the entirety of which is herein incorporated by reference), potato (Van der Voort et al., Mol. Gen. Genet. 255:438-447 (1997), the entirety of which is herein incorporated by reference; Meksem et al., Mol. Gen. Genet. 249:74-81 (1995), the entirety of which is herein incorporated by reference), Phytophthora infestans (Van der Lee et al., Fungal Genet. Biol. 21:278-291 (1997), the entirety of which is herein incorporated by reference), Bacillus anthracis (Keim et al, J. Bacteriol. 179:818-824 (1997), the entirety of which is herein incorporated by reference), Astragalus cremnophylax (Travis et al., Mol. Ecol. 5:735-745 (1996), the entirety of which is herein incorporated by reference), Arabidopsis (Cnops et al., Mol. Gen. Genet. 253:32-41 (1996), the entirety of which is herein incorporated by reference), Escherichia coli (Lin et al., Nucleic Acids Res. 24:3649-3650 (1996), the entirety of which is herein incorporated by reference), Aeromonas (Huys et al., Int. J. Syst. Bacteriol. 46:572-580 (1996), the entirety of which is herein incorporated by reference), nematode (Folkertsma et al., Mol. Plant. Microbe Interact. 9:47-54 (1996), the entirety of which is herein incorporated by reference), tomato (Thomas et al., Plant J. 8:785-794 (1995), the entirety of which is herein incorporated by reference) and human (Latorra et al., PCR Methods Appl. 3:351-358 (1994), the entirety of which is herein incorporated by reference). AFLP analysis has also been used for fingerprinting mRNA (Money et al., Nucleic Acids Res. 24:2616-2617 (1996), the entirety of which is herein incorporated by reference; Bachem et al., Plant J. 9:745-753 (1996), the entirety of which is herein incorporated by reference). It is understood that one or more of the nucleic acids of the present invention, may be utilized as markers or probes to detect polymorphisms by AFLP analysis or for fingerprinting RNA.

Polymorphisms may also be found using random amplified polymorphic DNA (RAPD) (Williams et al., Nucl. Acids Res. 18:6531-6535 (1990), the entirety of which is herein incorporated by reference) and cleaveable amplified polymorphic sequences (CAPS) (Lyamichev et al., Science 260:778-783 (1993), the entirety of which is herein incorporated by reference). It is understood that one or more of the nucleic acid molecules of the present invention, may be utilized as markers or probes to detect polymorphisms by RAPD or CAPS analysis.

Through genetic mapping, a fine scale linkage map can be developed using DNA markers and, then, a genomic DNA library of large-sized fragments can be screened with molecular markers linked to the desired trait. Molecular markers are advantageous for agronomic traits that are otherwise difficult to tag, such as resistance to pathogens, insects and nematodes, tolerance to abiotic stress, quality parameters and quantitative traits such as high yield potential.

The essential requirements for marker-assisted selection in a plant breeding program are: (1) the marker(s) should co-segregate or be closely linked with the desired trait; (2) an efficient means of screening large populations for the molecular marker(s) should be available; and (3) the screening technique should have high reproducibility across laboratories and preferably be economical to use and be user-friendly.

The genetic linkage of marker molecules can be established by a gene mapping model such as, without limitation, the flanking marker model reported by Lander and Botstein, Genetics 121:185-199 (1989) and the interval mapping, based on maximum likelihood methods described by Lander and Botstein, Genetics 121:185-199 (1989) and implemented in the software package MAPMAKER/QTL (Lincoln and Lander, Mapping Genes Controlling Quantitative Traits Using MAPMAKER/QTL, Whitehead Institute for Biomedical Research, Massachusetts, (1990). Additional software includes Qgene, Version 2.23 (1996), Department of Plant Breeding and Biometry, 266 Emerson Hall, Cornell University, Ithaca, N.Y., the manual of which is herein incorporated by reference in its entirety). Use of Qgene software is a particularly preferred approach.

A maximum likelihood estimate (MLE) for the presence of a marker is calculated, together with an MLE assuming no QTL effect, to avoid false positives. A log₁₀ of an odds ratio (LOD) is then calculated as: LOD=log₁₀ (MLE for the presence of a QTL/MLE given no linked QTL).

The LOD score essentially indicates how much more likely the data are to have arisen assuming the presence of a QTL than in its absence. The LOD threshold value for avoiding a false positive with a given confidence, say 95%, depends on the number of markers and the length of the genome. Graphs indicating LOD thresholds are set forth in Lander and Botstein, Genetics 121:185-199 (1989) the entirety of which is herein incorporated by reference and further described by Arús and Moreno-González, Plant Breeding, Hayward et al., (eds.) Chapman & Hall, London, pp. 314-331 (1993), the entirety of which is herein incorporated by reference.

Additional models can be used. Many modifications and alternative approaches to interval mapping have been reported, including the use non-parametric methods (Kruglyak and Lander, Genetics 139:1421-1428 (1995), the entirety of which is herein incorporated by reference). Multiple regression methods or models can be also be used, in which the trait is regressed on a large number of markers (Jansen, Biometrics in Plant Breeding, van Oijen and Jansen (eds.), Proceedings of the Ninth Meeting of the Eucarpia Section Biometrics in Plant Breeding, The Netherlands, pp. 116-124 (1994); Weber and Wricke, Advances in Plant Breeding, Blackwell, Berlin, 16 (1994), both of which is herein incorporated by reference in their entirety). Procedures combining interval mapping with regression analysis, whereby the phenotype is regressed onto a single putative QTL at a given marker interval and at the same time onto a number of markers that serve as ‘cofactors,’ have been reported by Jansen and Stam, Genetics 136:1447-1455 (1994), the entirety of which is herein incorporated by reference and Zeng, Genetics 136:1457-1468 (1994) the entirety of which is herein incorporated by reference. Generally, the use of cofactors reduces the bias and sampling error of the estimated QTL positions (Utz and Melchinger, Biometrics in Plant Breeding, van Oijen and Jansen (eds.) Proceedings of the Ninth Meeting of the Eucarpia Section Biometrics in Plant Breeding, The Netherlands, pp. 195-204 (1994), the entirety of which is herein incorporated by reference, thereby improving the precision and efficiency of QTL mapping (Zeng, Genetics 136:1457-1468 (1994)). These models can be extended to multi-environment experiments to analyze genotype-environment interactions (Jansen et al., Theo. Appl. Genet. 91:33-37 (1995), the entirety of which is herein incorporated by reference).

Selection of an appropriate mapping populations is important to map construction. The choice of appropriate mapping population depends on the type of marker systems employed (Tanksley et al., Molecular mapping plant chromosomes. Chromosome structure and function: Impact of new concepts, Gustafson and Appels (eds.), Plenum Press, New York, pp 157-173 (1988), the entirety of which is herein incorporated by reference). Consideration must be given to the source of parents (adapted vs. exotic) used in the mapping population. Chromosome pairing and recombination rates can be severely disturbed (suppressed) in wide crosses (adapted×exotic) and generally yield greatly reduced linkage distances. Wide crosses will usually provide segregating populations with a relatively large array of polymorphisms when compared to progeny in a narrow cross (adapted×adapted).

An F₂ population is the first generation of selfing after the hybrid seed is produced. Usually a single F₁ plant is selfed to generate a population segregating for all the genes in Mendelian (1:2:1) fashion. Maximum genetic information is obtained from a completely classified F₂ population using a codominant marker system (Mather, Measurement of Linkage in Heredity, Methuen and Co., (1938), the entirety of which is herein incorporated by reference). In the case of dominant markers, progeny tests (e.g. F₃, BCF₂) are required to identify the heterozygotes, thus making it equivalent to a completely classified F₂ population. However, this procedure is often prohibitive because of the cost and time involved in progeny testing. Progeny testing of F₂ individuals is often used in map construction where phenotypes do not consistently reflect genotype (e.g. disease resistance) or where trait expression is controlled by a QTL. Segregation data from progeny test populations (e.g. F₃ or BCF₂) can be used in map construction. Marker-assisted selection can then be applied to cross progeny based on marker-trait map associations (F₂, F₃), where linkage groups have not been completely disassociated by recombination events (i.e., maximum disequilibrium).

Recombinant inbred lines (RIL) (genetically related lines; usually >F₅, developed from continuously selfing F₂ lines towards homozygosity) can be used as a mapping population. Information obtained from dominant markers can be maximized by using RIL because all loci are homozygous or nearly so. Under conditions of tight linkage (i.e., about <10% recombination), dominant and co-dominant markers evaluated in RIL populations provide more information per individual than either marker type in backcross populations (Reiter et al., Proc. Natl. Acad. Sci. (U.S.A.) 89:1477-1481 (1992), the entirety of which is herein incorporated by reference). However, as the distance between markers becomes larger (i.e., loci become more independent), the information in RIL populations decreases dramatically when compared to codominant markers.

Backcross populations (e.g., generated from a cross between a successful variety (recurrent parent) and another variety (donor parent) carrying a trait not present in the former) can be utilized as a mapping population. A series of backcrosses to the recurrent parent can be made to recover most of its desirable traits. Thus a population is created consisting of individuals nearly like the recurrent parent but each individual carries varying amounts or mosaic of genomic regions from the donor parent. Backcross populations can be useful for mapping dominant markers if all loci in the recurrent parent are homozygous and the donor and recurrent parent have contrasting polymorphic marker alleles (Reiter et al., Proc. Natl. Acad. Sci. (U.S.A.) 89:1477-1481 (1992)). Information obtained from backcross populations using either codominant or dominant markers is less than that obtained from F₂ populations because one, rather than two, recombinant gametes are sampled per plant. Backcross populations, however, are more informative (at low marker saturation) when compared to RILs as the distance between linked loci increases in RIL populations (i.e. about 15% recombination). Increased recombination can be beneficial for resolution of tight linkages, but may be undesirable in the construction of maps with low marker saturation.

Near-isogenic lines (NIL) created by many backcrosses to produce an array of individuals that are nearly identical in genetic composition except for the trait or genomic region under interrogation can be used as a mapping population. In mapping with NILs, only a portion of the polymorphic loci are expected to map to a selected region.

Bulk segregant analysis (BSA) is a method developed for the rapid identification of linkage between markers and traits of interest (Michelmore et al., Proc. Natl. Acad. Sci. (U.S.A.) 88:9828-9832 (1991), the entirety of which is herein incorporated by reference). In BSA, two bulked DNA samples are drawn from a segregating population originating from a single cross. These bulks contain individuals that are identical for a particular trait (resistant or susceptible to particular disease) or genomic region but arbitrary at unlinked regions (i.e. heterozygous). Regions unlinked to the target region will not differ between the bulked samples of many individuals in BSA.

It is understood that one or more of the nucleic acid molecules of the present invention may be used as molecular markers. It is also understood that one or more of the protein molecules of the present invention may be used as molecular markers.

In accordance with this aspect of the present invention, a sample nucleic acid is obtained from plants cells or tissues. Any source of nucleic acid may be used. Preferably, the nucleic acid is genomic DNA. The nucleic acid is subjected to restriction endonuclease digestion. For example, one or more nucleic acid molecule or fragment thereof of the present invention can be used as a probe in accordance with the above-described polymorphic methods. The polymorphism obtained in this approach can then be cloned to identify the mutation at the coding region which alters the protein's structure or regulatory region of the gene which affects its expression level.

In an aspect of the present invention, one or more of the nucleic molecules of the present invention are used to determine the level (i.e., the concentration of mRNA in a sample, etc.) in a plant (preferably maize or soybean) or pattern (i.e., the kinetics of expression, rate of decomposition, stability profile, etc.) of the expression of a protein encoded in part or whole by one or more of the nucleic acid molecule of the present invention (collectively, the “Expression Response” of a cell or tissue). As used herein, the Expression Response manifested by a cell or tissue is said to be “altered” if it differs from the Expression Response of cells or tissues of plants not exhibiting the phenotype. To determine whether an Expression Response is altered, the Expression Response manifested by the cell or tissue of the plant exhibiting the phenotype is compared with that of a similar cell or tissue sample of a plant not exhibiting the phenotype. As will be appreciated, it is not necessary to re-determine the Expression Response of the cell or tissue sample of plants not exhibiting the phenotype each time such a comparison is made; rather, the Expression Response of a particular plant may be compared with previously obtained values of normal plants. As used herein, the phenotype of the organism is any of one or more characteristics of an organism (e.g. disease resistance, pest tolerance, environmental tolerance such as tolerance to abiotic stress, male sterility, quality improvement or yield etc.). A change in genotype or phenotype may be transient or permanent. Also as used herein, a tissue sample is any sample that comprises more than one cell. In a preferred aspect, a tissue sample comprises cells that share a common characteristic (e.g. derived from root, seed, flower, leaf, stem or pollen etc.).

In one aspect of the present invention, an evaluation can be conducted to determine whether a particular mRNA molecule is present. One or more of the nucleic acid molecules of the present invention, preferably one or more of the EST nucleic acid molecules or fragments thereof of the present invention are utilized to detect the presence or quantity of the mRNA species. Such molecules are then incubated with cell or tissue extracts of a plant under conditions sufficient to permit nucleic acid hybridization. The detection of double-stranded probe-mRNA hybrid molecules is indicative of the presence of the mRNA; the amount of such hybrid formed is proportional to the amount of mRNA. Thus, such probes may be used to ascertain the level and extent of the mRNA production in a plant's cells or tissues. Such nucleic acid hybridization may be conducted under quantitative conditions (thereby providing a numerical value of the amount of the mRNA present). Alternatively, the assay may be conducted as a qualitative assay that indicates either that the mRNA is present, or that its level exceeds a user set, predefined value.

A principle of in situ hybridization is that a labeled, single-stranded nucleic acid probe will hybridize to a complementary strand of cellular DNA or RNA and, under the appropriate conditions, these molecules will form a stable hybrid. When nucleic acid hybridization is combined with histological techniques, specific DNA or RNA sequences can be identified within a single cell. An advantage of in situ hybridization over more conventional techniques for the detection of nucleic acids is that it allows an investigator to determine the precise spatial population (Angerer et al., Dev. Biol. 101:477-484 (1984), the entirety of which is herein incorporated by reference; Angerer et al., Dev. Biol. 112:157-166 (1985), the entirety of which is herein incorporated by reference; Dixon et al., EMBO J. 10:1317-1324 (1991), the entirety of which is herein incorporated by reference). In situ hybridization may be used to measure the steady-state level of RNA accumulation. It is a sensitive technique and RNA sequences present in as few as 5-10 copies per cell can be detected (Hardin et al., J. Mol. Biol. 202:417-431 (1989), the entirety of which is herein incorporated by reference). A number of protocols have been devised for in situ hybridization, each with tissue preparation, hybridization and washing conditions (Meyerowitz, Plant Mol. Biol. Rep. 5:242-250 (1987), the entirety of which is herein incorporated by reference; Cox and Goldberg, In: Plant Molecular Biology: A Practical Approach, Shaw (ed.), pp 1-35, IRL Press, Oxford (1988), the entirety of which is herein incorporated by reference; Raikhel et al., In situ RNA hybridization in plant tissues, In: Plant Molecular Biology Manual, vol. B9:1-32, Kluwer Academic Publisher, Dordrecht, Belgium (1989), the entirety of which is herein incorporated by reference).

In situ hybridization also allows for the localization of proteins within a tissue or cell (Wilkinson, In Situ Hybridization, Oxford University Press, Oxford (1992), the entirety of which is herein incorporated by reference; Langdale, In Situ Hybridization In: The Maize Handbook, Freeling and Walbot (eds.), pp 165-179, Springer-Verlag, New York (1994), the entirety of which is herein incorporated by reference). It is understood that one or more of the molecules of the present invention, preferably one or more of the EST nucleic acid molecules or fragments thereof of the present invention or one or more of the antibodies of the present invention may be utilized to detect the level or pattern of a carbon assimilation pathway enzyme or mRNA thereof by in situ hybridization.

Fluorescent in situ hybridization allows the localization of a particular DNA sequence along a chromosome which is useful, among other uses, for gene mapping, following chromosomes in hybrid lines or detecting chromosomes with translocations, transversions or deletions. In situ hybridization has been used to identify chromosomes in several plant species (Griffor et al., Plant Mol. Biol. 17:101-109 (1991), the entirety of which is herein incorporated by reference; Gustafson et al., Proc. Natl. Acad. Sci. (U.S.A.) 87:1899-1902 (1990), herein incorporated by reference; Mukai and Gill, Genome 34:448-452 (1991), the entirety of which is herein incorporated by reference; Schwarzacher and Heslop-Harrison, Genome 34:317-323 (1991); Wang et al., Jpn. J. Genet. 66:313-316 (1991), the entirety of which is herein incorporated by reference; Parra and Windle, Nature Genetics 5:17-21 (1993), the entirety of which is herein incorporated by reference). It is understood that the nucleic acid molecules of the present invention may be used as probes or markers to localize sequences along a chromosome.

Another method to localize the expression of a molecule is tissue printing. Tissue printing provides a way to screen, at the same time on the same membrane many tissue sections from different plants or different developmental stages. Tissue-printing procedures utilize films designed to immobilize proteins and nucleic acids. In essence, a freshly cut section of a tissue is pressed gently onto nitrocellulose paper, nylon membrane or polyvinylidene difluoride membrane. Such membranes are commercially available (e.g. Millipore, Bedford, Mass. U.S.A.). The contents of the cut cell transfer onto the membrane and the contents and are immobilized to the membrane. The immobilized contents form a latent print that can be visualized with appropriate probes. When a plant tissue print is made on nitrocellulose paper, the cell walls leave a physical print that makes the anatomy visible without further treatment (Varner and Taylor, Plant Physiol. 91:31-33 (1989), the entirety of which is herein incorporated by reference).

Tissue printing on substrate films is described by Daoust, Exp. Cell Res. 12:203-211 (1957), the entirety of which is herein incorporated by reference, who detected amylase, protease, ribonuclease and deoxyribonuclease in animal tissues using starch, gelatin and agar films. These techniques can be applied to plant tissues (Yomo and Taylor, Planta 112:35-43 (1973); the entirety of which is herein incorporated by reference; Harris and Chrispeels, Plant Physiol. 56:292-299 (1975), the entirety of which is herein incorporated by reference). Advances in membrane technology have increased the range of applications of Daoust's tissue-printing techniques allowing (Cassab and Varner, J. Cell. Biol. 105:2581-2588 (1987), the entirety of which is herein incorporated by reference) the histochemical localization of various plant enzymes and deoxyribonuclease on nitrocellulose paper and nylon (Spruce et al, Phytochemistry 26:2901-2903 (1987), the entirety of which is herein incorporated by reference; Barres et al, Neuron 5:527-544 (1990), the entirety of which is herein incorporated by reference; Reid and Pont-Lezica, Tissue Printing: Tools for the Study of Anatomy, Histochemistry and Gene Expression, Academic Press, New York, N.Y. (1992), the entirety of which is herein incorporated by reference; Reid et al., Plant Physiol. 93: 160-165 (1990), the entirety of which is herein incorporated by reference; Ye et al, Plant J. 1:175-183 (1991), the entirety of which is herein incorporated by reference).

It is understood that one or more of the molecules of the present invention, preferably one or more of the EST nucleic acid molecules or fragments thereof of the present invention or one or more of the antibodies of the present invention may be utilized to detect the presence or quantity of a carbon assimilation pathway enzyme by tissue printing.

Further it is also understood that any of the nucleic acid molecules of the present invention may be used as marker nucleic acids and or probes in connection with methods that require probes or marker nucleic acids. As used herein, a probe is an agent that is utilized to determine an attribute or feature (e.g. presence or absence, location, correlation, etc.) of a molecule, cell, tissue or plant. As used herein, a marker nucleic acid is a nucleic acid molecule that is utilized to determine an attribute or feature (e.g., presence or absence, location, correlation, etc.) or a molecule, cell, tissue or plant.

A microarray-based method for high-throughput monitoring of plant gene expression may be utilized to measure gene-specific hybridization targets. This ‘chip’-based approach involves using microarrays of nucleic acid molecules as gene-specific hybridization targets to quantitatively measure expression of the corresponding plant genes (Schena et al., Science 270:467-470 (1995), the entirety of which is herein incorporated by reference; Shalon, Ph.D. Thesis, Stanford University (1996), the entirety of which is herein incorporated by reference). Every nucleotide in a large sequence can be queried at the same time. Hybridization can be used to efficiently analyze nucleotide sequences.

Several microarray methods have been described. One method compares the sequences to be analyzed by hybridization to a set of oligonucleotides representing all possible subsequences (Bains and Smith, J. Theor. Biol. 135:303-307 (1989), the entirety of which is herein incorporated by reference). A second method hybridizes the sample to an array of oligonucleotide or cDNA molecules. An array consisting of oligonucleotides complementary to subsequences of a target sequence can be used to determine the identity of a target sequence, measure its amount and detect differences between the target and a reference sequence. Nucleic acid molecules microarrays may also be screened with protein molecules or fragments thereof to determine nucleic acid molecules that specifically bind protein molecules or fragments thereof.

The microarray approach may be used with polypeptide targets (U.S. Pat. No. 5,445,934; U.S. Pat. No. 5,143,854; U.S. Pat. No. 5,079,600; U.S. Pat. No. 4,923,901, all of which are herein incorporated by reference in their entirety). Essentially, polypeptides are synthesized on a substrate (microarray) and these polypeptides can be screened with either protein molecules or fragments thereof or nucleic acid molecules in order to screen for either protein molecules or fragments thereof or nucleic acid molecules that specifically bind the target polypeptides. (Fodor et al., Science 251:767-773 (1991), the entirety of which is herein incorporated by reference). It is understood that one or more of the nucleic acid molecules or protein or fragments thereof of the present invention may be utilized in a microarray based method.

In a preferred embodiment of the present invention microarrays may be prepared that comprise nucleic acid molecules where such nucleic acid molecules encode at least one, preferably at least two, more preferably at least three carbon assimilation pathway enzymes, more preferably at least four carbon assimilation pathway enzymes, more preferably at least five carbon assimilation pathway enzymes, more preferably at least six carbon assimilation pathway enzymes, more preferably at least seven carbon assimilation pathway enzymes, more preferably at least eight carbon assimilation pathway enzymes, more preferably at least nine carbon assimilation pathway enzymes, more preferably at least ten carbon assimilation pathway enzymes, more preferably at least eleven carbon assimilation pathway enzymes, more preferably at least twelve carbon assimilation pathway enzymes, more preferably at least thirteen carbon assimilation pathway enzymes, more preferably at least fourteen carbon assimilation pathway enzymes, more preferably at least fifteen carbon assimilation pathway enzymes, more preferably at least sixteen carbon assimilation pathway enzymes, more preferably at least seventeen carbon assimilation pathway enzymes, more preferably at least eighteen carbon assimilation pathway enzymes, more preferably at least nineteen carbon assimilation pathway enzymes, more preferably at least twenty carbon assimilation pathway enzymes, more preferably at least twenty one carbon assimilation pathway enzymes, more preferably at least twenty two carbon assimilation pathway enzymes, more preferably at least twenty three carbon assimilation pathway enzymes, more preferably at least twenty four carbon assimilation pathway enzymes and even more preferably at least twenty five carbon assimilation pathway enzymes. In a preferred embodiment the nucleic acid molecules are selected from the group consisting of a nucleic acid molecule that encodes a maize or soybean ribulose-bisphosphate carboxylase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean phosphoglycerate kinase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean glyceraldehyde 3-phosphate dehydrogenase enzyme or fragment thereof, a nucleic acid molecule that encodes a putative maize glyceraldehyde 3-phosphate dehydrogenase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean triose phosphate isomerase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean aldolase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean fructose-1,6-bisphosphatase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean transketolase enzyme or fragment thereof, a nucleic acid molecule that encodes a putative maize or soybean transketolase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean sedoheptulose-1,7-bisphosphatase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean D-ribulose-5-phosphate-3-epimerase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean ribose-5-phosphate isomerase enzyme or fragment thereof, a nucleic acid molecule that encodes a putative maize or soybean ribose-5-phosphate isomerase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean ribose-5-phosphate kinase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean phosphoenolpyruvate carboxylase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean NADP-dependent malate dehydrogenase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean aspartate aminotransferase enzyme or fragment thereof, a nucleic acid molecule that encodes a putative maize or soybean aspartate aminotransferase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean alanine aminotransferase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean NADP-dependent malic enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean NAD-dependent malic enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean PEP carboxykinase enzyme or fragment thereof, a nucleic acid molecule that encodes a putative soybean PEP carboxykinase enzyme or fragment thereof, a nucleic acid molecule that encodes a maize or soybean pyruvate, phosphate dikinase enzyme or fragment thereof and a nucleic acid molecule that encodes a maize or soybean pyrophosphatase enzyme or fragment thereof.

Site directed mutagenesis may be utilized to modify nucleic acid sequences, particularly as it is a technique that allows one or more of the amino acids encoded by a nucleic acid molecule to be altered (e.g. a threonine to be replaced by a methionine). Three basic methods for site directed mutagenesis are often employed. These are cassette mutagenesis (Wells et al., Gene 34:315-323 (1985), the entirety of which is herein incorporated by reference), primer extension (Gilliam et al., Gene 12:129-137 (1980), the entirety of which is herein incorporated by reference; Zoller and Smith, Methods Enzymol. 100:468-500 (1983), the entirety of which is herein incorporated by reference; Dalbadie-McFarland et al., Proc. Natl. Acad. Sci. (U.S.A.) 79:6409-6413 (1982), the entirety of which is herein incorporated by reference) and methods based upon PCR (Scharf et al., Science 233:1076-1078 (1986), the entirety of which is herein incorporated by reference; Higuchi et al., Nucleic Acids Res. 16:7351-7367 (1988), the entirety of which is herein incorporated by reference). Site directed mutagenesis approaches are also described in European Patent 0 385 962, the entirety of which is herein incorporated by reference; European Patent 0 359 472, the entirety of which is herein incorporated by reference; and PCT Patent Application WO 93/07278, the entirety of which is herein incorporated by reference.

Site directed mutagenesis strategies have been applied to plants for both in vitro as well as in vivo site directed mutagenesis (Lanz et al., J. Biol. Chem. 266:9971-9976 (1991), the entirety of which is herein incorporated by reference; Kovgan and Zhdanov, Biotekhnologiya 5:148-154; No. 207160n, Chemical Abstracts 110:225 (1989), the entirety of which is herein incorporated by reference; Ge et al., Proc. Natl. Acad. Sci. (U.S.A.) 86:4037-4041 (1989), the entirety of which is herein incorporated by reference; Zhu et al., J. Biol. Chem. 271:18494-18498 (1996), the entirety of which is herein incorporated by reference; Chu et al., Biochemistry 33:6150-6157 (1994), the entirety of which is herein incorporated by reference; Small et al., EMBO J. 11:1291-1296 (1992), the entirety of which is herein incorporated by reference; Cho et al., Mol. Biotechnol. 8:13-16 (1997), the entirety of which is herein incorporated by reference; Kita et al., J. Biol. Chem. 271:26529-26535 (1996), the entirety of which is herein incorporated by reference, Jin et al., Mol. Microbiol. 7:555-562 (1993), the entirety of which is herein incorporated by reference; Hatfield and Vierstra, J. Biol. Chem. 267:14799-14803 (1992), the entirety of which is herein incorporated by reference; Zhao et al., Biochemistry 31:5093-5099 (1992), the entirety of which is herein incorporated by reference).

Any of the nucleic acid molecules of the present invention may either be modified by site directed mutagenesis or used as, for example, nucleic acid molecules that are used to target other nucleic acid molecules for modification. It is understood that mutants with more than one altered nucleotide can be constructed using techniques that practitioners are familiar with such as isolating restriction fragments and ligating such fragments into an expression vector (see, for example, Sambrook et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Press (1989)).

Sequence-specific DNA-binding proteins play a role in the regulation of transcription. The isolation of recombinant cDNAs encoding these proteins facilitates the biochemical analysis of their structural and functional properties. Genes encoding such DNA-binding proteins have been isolated using classical genetics (Vollbrecht et al., Nature 350: 241-243 (1991), the entirety of which is herein incorporated by reference) and molecular biochemical approaches, including the screening of recombinant cDNA libraries with antibodies (Landschulz et al., Genes Dev. 2:786-800 (1988), the entirety of which is herein incorporated by reference) or DNA probes (Bodner et al., Cell 55:505-518 (1988), the entirety of which is herein incorporated by reference). In addition, an in situ screening procedure has been used and has facilitated the isolation of sequence-specific DNA-binding proteins from various plant species (Gilmartin et al., Plant Cell 4:839-849 (1992), the entirety of which is herein incorporated by reference; Schindler et al., EMBO J. 11:1261-1273 (1992), the entirety of which is herein incorporated by reference). An in situ screening protocol does not require the purification of the protein of interest (Vinson et al., Genes Dev. 2:801-806 (1988), the entirety of which is herein incorporated by reference; Singh et al., Cell 52:415-423 (1988), the entirety of which is herein incorporated by reference).

Two steps may be employed to characterize DNA-protein interactions. The first is to identify promoter fragments that interact with DNA-binding proteins, to titrate binding activity, to determine the specificity of binding and to determine whether a given DNA-binding activity can interact with related DNA sequences (Sambrook et al., Molecular Cloning: A Laboratory Manual, 2^(nd) edition, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. (1989)). Electrophoretic mobility-shift assay is a widely used assay. The assay provides a rapid and sensitive method for detecting DNA-binding proteins based on the observation that the mobility of a DNA fragment through a nondenaturing, low-ionic strength polyacrylamide gel is retarded upon association with a DNA-binding protein (Fried and Crother, Nucleic Acids Res. 9:6505-6525 (1981), the entirety of which is herein incorporated by reference). When one or more specific binding activities have been identified, the exact sequence of the DNA bound by the protein may be determined. Several procedures for characterizing protein/DNA-binding sites are used, including methylation and ethylation interference assays (Maxam and Gilbert, Methods Enzymol. 65:499-560 (1980), the entirety of which is herein incorporated by reference; Wissman and Hillen, Methods Enzymol. 208:365-379 (1991), the entirety of which is herein incorporated by reference), footprinting techniques employing DNase I (Galas and Schmitz, Nucleic Acids Res. 5:3157-3170 (1978), the entirety of which is herein incorporated by reference), 1,10-phenanthroline-copper ion methods (Sigman et al., Methods Enzymol. 208:414-433 (1991), the entirety of which is herein incorporated by reference) and hydroxyl radicals methods (Dixon et al., Methods Enzymol. 208:414-433 (1991), the entirety of which is herein incorporated by reference). It is understood that one or more of the nucleic acid molecules of the present invention may be utilized to identify a protein or fragment thereof that specifically binds to a nucleic acid molecule of the present invention. It is also understood that one or more of the protein molecules or fragments thereof of the present invention may be utilized to identify a nucleic acid molecule that specifically binds to it.

A two-hybrid system is based on the fact that many cellular functions are carried out by proteins, such as transcription factors, that interact (physically) with one another. Two-hybrid systems have been used to probe the function of new proteins (Chien et al., Proc. Natl. Acad. Sci. (U.S.A.) 88:9578-9582 (1991) the entirety of which is herein incorporated by reference; Durfee et al., Genes Dev. 7:555-569 (1993) the entirety of which is herein incorporated by reference; Choi et al., Cell 78:499-512 (1994), the entirety of which is herein incorporated by reference; Kranz et al., Genes Dev. 8:313-327 (1994), the entirety of which is herein incorporated by reference).

Interaction mating techniques have facilitated a number of two-hybrid studies of protein-protein interaction. Interaction mating has been used to examine interactions between small sets of tens of proteins (Finley and Brent, Proc. Natl. Acad. Sci. (U.S.A.) 91:12098-12984 (1994), the entirety of which is herein incorporated by reference), larger sets of hundreds of proteins (Bendixen et al., Nucl. Acids Res. 22:1778-1779 (1994), the entirety of which is herein incorporated by reference) and to comprehensively map proteins encoded by a small genome (Bartel et al., Nature Genetics 12:72-77 (1996), the entirety of which is herein incorporated by reference). This technique utilizes proteins fused to the DNA-binding domain and proteins fused to the activation domain. They are expressed in two different haploid yeast strains of opposite mating type and the strains are mated to determine if the two proteins interact. Mating occurs when haploid yeast strains come into contact and result in the fusion of the two haploids into a diploid yeast strain. An interaction can be determined by the activation of a two-hybrid reporter gene in the diploid strain. An advantage of this technique is that it reduces the number of yeast transformations needed to test individual interactions. It is understood that the protein-protein interactions of protein or fragments thereof of the present invention may be investigated using the two-hybrid system and that any of the nucleic acid molecules of the present invention that encode such proteins or fragments thereof may be used to transform yeast in the two-hybrid system.

(a) Plant Constructs and Plant Transformants

One or more of the nucleic acid molecules of the present invention may be used in plant transformation or transfection. Exogenous genetic material may be transferred into a plant cell and the plant cell regenerated into a whole, fertile or sterile plant. Exogenous genetic material is any genetic material, whether naturally occurring or otherwise, from any source that is capable of being inserted into any organism. Such genetic material may be transferred into either monocotyledons and dicotyledons including, but not limited to maize (pp 63-69), soybean (pp 50-60), Arabidopsis (p 45), phaseolus (pp 47-49), peanut (pp 49-50), alfalfa (p 60), wheat (pp 69-71), rice (pp 72-79), oat (pp 80-81), sorghum (p 83), rye (p 84), tritordeum (p 84), millet (p 85), fescue (p 85), perennial ryegrass (p 86), sugarcane (p 87), cranberry (p 101), papaya (pp 101-102), banana (p 103), banana (p 103), muskmelon (p 104), apple (p 104), cucumber (p 105), dendrobium (p 109), gladiolus (p 110), chrysanthemum (p 110), liliacea (p 111), cotton (pp 113-114), eucalyptus (p 115), sunflower (p 118), canola (p 118), turfgrass (p 121), sugarbeet (p 122), coffee (p 122) and dioscorea (p 122), (Christou, In: Particle Bombardment for Genetic Engineering of Plants, Biotechnology Intelligence Unit. Academic Press, San Diego, Calif. (1996), the entirety of which is herein incorporated by reference).

Transfer of a nucleic acid that encodes for a protein can result in overexpression of that protein in a transformed cell or transgenic plant. One or more of the proteins or fragments thereof encoded by nucleic acid molecules of the present invention may be overexpressed in a transformed cell or transformed plant. Particularly, any of the carbon assimilation pathway enzymes or fragments thereof may be overexpressed in a transformed cell or transgenic plant. Such overexpression may be the result of transient or stable transfer of the exogenous genetic material.

Exogenous genetic material may be transferred into a plant cell and the plant cell by the use of a DNA vector or construct designed for such a purpose. Design of such a vector is generally within the skill of the art (See, Plant Molecular Biology: A Laboratory Manual, Clark (ed.), Springier, New York (1997), the entirety of which is herein incorporated by reference).

A construct or vector may include a plant promoter to express the protein or protein fragment of choice. A number of promoters which are active in plant cells have been described in the literature. These include the nopaline synthase (NOS) promoter (Ebert et al., Proc. Natl. Acad. Sci. (U.S.A.) 84:5745-5749 (1987), the entirety of which is herein incorporated by reference), the octopine synthase (OCS) promoter (which are carried on tumor-inducing plasmids of Agrobacterium tumefaciens), the caulimovirus promoters such as the cauliflower mosaic virus (CaMV) 19S promoter (Lawton et al., Plant Mol. Biol. 9:315-324 (1987), the entirety of which is herein incorporated by reference) and the CAMV 35S promoter (Odell et al., Nature 313:810-812 (1985), the entirety of which is herein incorporated by reference), the figwort mosaic virus 35S-promoter, the light-inducible promoter from the small subunit of ribulose-1,5-bis-phosphate carboxylase (ssRUBISCO), the Adh promoter (Walker et al., Proc. Natl. Acad. Sci. (U.S.A.) 84:6624-6628 (1987), the entirety of which is herein incorporated by reference), the sucrose synthase promoter (Yang et al., Proc. Natl. Acad. Sci. (U.S.A.) 87:4144-4148 (1990), the entirety of which is herein incorporated by reference), the R gene complex promoter (Chandler et al., The Plant Cell 1: 1175-1183 (1989), the entirety of which is herein incorporated by reference) and the chlorophyll a/b binding protein gene promoter, etc. These promoters have been used to create DNA constructs which have been expressed in plants; see, e.g., PCT publication WO 84/02913, herein incorporated by reference in its entirety.

Promoters which are known or are found to cause transcription of DNA in plant cells can be used in the present invention. Such promoters may be obtained from a variety of sources such as plants and plant viruses. It is preferred that the particular promoter selected should be capable of causing sufficient expression to result in the production of an effective amount of the carbon assimilation pathway enzyme to cause the desired phenotype. In addition to promoters that are known to cause transcription of DNA in plant cells, other promoters may be identified for use in the current invention by screening a plant cDNA library for genes which are selectively or preferably expressed in the target tissues or cells.

For the purpose of expression in source tissues of the plant, such as the leaf, seed, root or stem, it is preferred that the promoters utilized in the present invention have relatively high expression in these specific tissues. For this purpose, one may choose from a number of promoters for genes with tissue- or cell-specific or -enhanced expression. Examples of such promoters reported in the literature include the chloroplast glutamine synthetase GS2 promoter from pea (Edwards et al., Proc. Natl. Acad. Sci. (U.S.A.). 87:3459-3463 (1990), herein incorporated by reference in its entirety), the chloroplast fructose-1,6-biphosphatase (FBPase) promoter from wheat (Lloyd et al., Mol. Gen. Genet. 225:209-216 (1991), herein incorporated by reference in its entirety), the nuclear photosynthetic ST-LS1 promoter from potato (Stockhaus et al., EMBO J. 8:2445-2451 (1989), herein incorporated by reference in its entirety), the serine/threonine kinase (PAL) promoter and the glucoamylase (CHS) promoter from Arabidopsis thaliana. Also reported to be active in photosynthetically active tissues are the ribulose-1,5-bisphosphate carboxylase (RbcS) promoter from eastern larch (Larix laricina), the promoter for the cab gene, cab6, from pine (Yamamoto et al., Plant Cell Physiol. 35:773-778 (1994), herein incorporated by reference in its entirety), the promoter for the Cab-1 gene from wheat (Fejes et al., Plant Mol. Biol. 15:921-932 (1990), herein incorporated by reference in its entirety), the promoter for the CAB-1 gene from spinach (Lubberstedt et al., Plant Physiol. 104:997-1006 (1994), herein incorporated by reference in its entirety), the promoter for the cab1R gene from rice (Luan et al., Plant Cell. 4:971-981 (1992), the entirety of which is herein incorporated by reference), the pyruvate, orthophosphate dikinase (PPDK) promoter from maize (Matsuoka et al., Proc. Natl. Acad. Sci. (U.S.A.) 90: 9586-9590 (1993), herein incorporated by reference in its entirety), the promoter for the tobacco Lhcb1*2 gene (Cerdan et al., Plant Mol. Biol. 33:245-255 (1997), herein incorporated by reference in its entirety), the Arabidopsis thaliana SUC2 sucrose-H+ symporter promoter (Truernit et al., Planta. 196:564-570 (1995), herein incorporated by reference in its entirety) and the promoter for the thylakoid membrane proteins from spinach (psaD, psaF, psaE, PC, FNR, atpC, atpD, cab, rbcS). Other promoters for the chlorophyll a/b-binding proteins may also be utilized in the present invention, such as the promoters for LhcB gene and PsbP gene from white mustard (Sinapis alba; Kretsch et al., Plant Mol. Biol. 28:219-229 (1995), the entirety of which is herein incorporated by reference).

For the purpose of expression in sink tissues of the plant, such as the tuber of the potato plant, the fruit of tomato, or the seed of maize, wheat, rice and barley, it is preferred that the promoters utilized in the present invention have relatively high expression in these specific tissues. A number of promoters for genes with tuber-specific or -enhanced expression are known, including the class I patatin promoter (Bevan et al., EMBO J. 8:1899-1906 (1986); Jefferson et al., Plant Mol. Biol. 14:995-1006 (1990), both of which are herein incorporated by reference in its entirety), the promoter for the potato tuber ADPGPP genes, both the large and small subunits, the sucrose synthase promoter (Salanoubat and Belliard, Gene. 60:47-56 (1987), Salanoubat and Belliard, Gene. 84:181-185 (1989), both of which are incorporated by reference in their entirety), the promoter for the major tuber proteins including the 22 kd protein complexes and proteinase inhibitors (Hannapel, Plant Physiol. 101:703-704 (1993), herein incorporated by reference in its entirety), the promoter for the granule bound starch synthase gene (GBSS) (Visser et al., Plant Mol. Biol. 17:691-699 (1991), herein incorporated by reference in its entirety) and other class I and II patatins promoters (Koster-Topfer et al., Mol Gen Genet. 219:390-396 (1989); Mignery et al., Gene. 62:27-44 (1988), both of which are herein incorporated by reference in their entirety).

Other promoters can also be used to express a carbon assimilation pathway enzyme or fragment thereof in specific tissues, such as seeds or fruits. The promoter for β-conglycinin (Chen et al., Dev. Genet. 10: 112-122 (1989), herein incorporated by reference in its entirety) or other seed-specific promoters such as the napin and phaseolin promoters, can be used. The zeins are a group of storage proteins found in maize endosperm. Genomic clones for zein genes have been isolated (Pedersen et al., Cell 29:1015-1026 (1982), herein incorporated by reference in its entirety) and the promoters from these clones, including the 15 kD, 16 kD, 19 kD, 22 kD, 27 kD and genes, could also be used. Other promoters known to function, for example, in maize include the promoters for the following genes: waxy, Brittle, Shrunken 2, Branching enzymes I and II, starch synthases, debranching enzymes, oleosins, glutelins and sucrose synthases. A particularly preferred promoter for maize endosperm expression is the promoter for the glutelin gene from rice, more particularly the Osgt-1 promoter (Zheng et al., Mol. Cell. Biol. 13:5829-5842 (1993), herein incorporated by reference in its entirety). Examples of promoters suitable for expression in wheat include those promoters for the ADPglucose pyrosynthase (ADPGPP) subunits, the granule bound and other starch synthase, the branching and debranching enzymes, the embryogenesis-abundant proteins, the gliadins and the glutenins. Examples of such promoters in rice include those promoters for the ADPGPP subunits, the granule bound and other starch synthase, the branching enzymes, the debranching enzymes, sucrose synthases and the glutelins. A particularly preferred promoter is the promoter for rice glutelin, Osgt-1. Examples of such promoters for barley include those for the ADPGPP subunits, the granule bound and other starch synthase, the branching enzymes, the debranching enzymes, sucrose synthases, the hordeins, the embryo globulins and the aleurone specific proteins.

Root specific promoters may also be used. An example of such a promoter is the promoter for the acid chitinase gene (Samac et al., Plant Mol. Biol. 25:587-596 (1994), the entirety of which is herein incorporated by reference). Expression in root tissue could also be accomplished by utilizing the root specific subdomains of the CaMV35S promoter that have been identified (Lam et al., Proc. Natl. Acad. Sci. (U.S.A.) 86:7890-7894 (1989), herein incorporated by reference in its entirety). Other root cell specific promoters include those reported by Conkling et al. (Conkling et al., Plant Physiol. 93:1203-1211 (1990), the entirety of which is herein incorporated by reference).

Additional promoters that may be utilized are described, for example, in U.S. Pat. Nos. 5,378,619; 5,391,725; 5,428,147; 5,447,858; 5,608,144; 5,608,144; 5,614,399; 5,633,441; 5,633,435; and 4,633,436, all of which are herein incorporated in their entirety. In addition, a tissue specific enhancer may be used (Fromm et al., The Plant Cell 1:977-984 (1989), the entirety of which is herein incorporated by reference).

Constructs or vectors may also include with the coding region of interest a nucleic acid sequence that acts, in whole or in part, to terminate transcription of that region. For example, such sequences have been isolated including the Tr7 3′ sequence and the NOS 3′ sequence (Ingelbrecht et al., The Plant Cell 1:671-680 (1989), the entirety of which is herein incorporated by reference; Bevan et al., Nucleic Acids Res. 11:369-385 (1983), the entirety of which is herein incorporated by reference), or the like.

A vector or construct may also include regulatory elements. Examples of such include the Adh intron 1 (Callis et al., Genes and Develop. 1:1183-1200 (1987), the entirety of which is herein incorporated by reference), the sucrose synthase intron (Vasil et al., Plant Physiol. 91:1575-1579 (1989), the entirety of which is herein incorporated by reference) and the TMV omega element (Gallie et al., The Plant Cell 1:301-311 (1989), the entirety of which is herein incorporated by reference). These and other regulatory elements may be included when appropriate.

A vector or construct may also include a selectable marker. Selectable markers may also be used to select for plants or plant cells that contain the exogenous genetic material. Examples of such include, but are not limited to, a neo gene (Potrykus et al., Mol. Gen. Genet. 199:183-188 (1985), the entirety of which is herein incorporated by reference) which codes for kanamycin resistance and can be selected for using kanamycin, G418, etc.; a bar gene which codes for bialaphos resistance; a mutant EPSP synthase gene (Hinchee et al., Bio/Technology 6:915-922 (1988), the entirety of which is herein incorporated by reference) which encodes glyphosate resistance; a nitrilase gene which confers resistance to bromoxynil (Stalker et al., J. Biol. Chem. 263:6310-6314 (1988), the entirety of which is herein incorporated by reference); a mutant acetolactate synthase gene (ALS) which confers imidazolinone or sulphonylurea resistance (European Patent Application 154,204 (Sep. 11, 1985), the entirety of which is herein incorporated by reference); and a methotrexate resistant DHFR gene (Thillet et al., J. Biol. Chem. 263:12500-12508 (1988), the entirety of which is herein incorporated by reference).

A vector or construct may also include a transit peptide. Incorporation of a suitable chloroplast transit peptide may also be employed (European Patent Application Publication Number 0218571, the entirety of which is herein incorporated by reference). Translational enhancers may also be incorporated as part of the vector DNA. DNA constructs could contain one or more 5′ non-translated leader sequences which may serve to enhance expression of the gene products from the resulting mRNA transcripts. Such sequences may be derived from the promoter selected to express the gene or can be specifically modified to increase translation of the mRNA. Such regions may also be obtained from viral RNAs, from suitable eukaryotic genes, or from a synthetic gene sequence. For a review of optimizing expression of transgenes, see Koziel et al., Plant Mol. Biol. 32:393-405 (1996), the entirety of which is herein incorporated by reference.

A vector or construct may also include a screenable marker. Screenable markers may be used to monitor expression. Exemplary screenable markers include a β-glucuronidase or uidA gene (GUS) which encodes an enzyme for which various chromogenic substrates are known (Jefferson, Plant Mol. Biol, Rep. 5:387-405 (1987), the entirety of which is herein incorporated by reference; Jefferson et al., EMBO J. 6:3901-3907 (1987), the entirety of which is herein incorporated by reference); an R-locus gene, which encodes a product that regulates the production of anthocyanin pigments (red color) in plant tissues (Dellaporta et al., Stadler Symposium 11:263-282 (1988), the entirety of which is herein incorporated by reference); a lactamase gene (Sutcliffe et al., Proc. Natl. Acad. Sci. (U.S.A.) 75:3737-3741 (1978), the entirety of which is herein incorporated by reference), a gene which encodes an enzyme for which various chromogenic substrates are known (e.g., PADAC, a chromogenic cephalosporin); a luciferase gene (Ow et al., Science 234:856-859 (1986), the entirety of which is herein incorporated by reference); a xylE gene (Zukowsky et al., Proc. Natl. Acad. Sci. (U.S.A.) 80:1101-1105 (1983), the entirety of which is herein incorporated by reference) which encodes a catechol diozygenase that can convert chromogenic catechols; an α-amylase gene (Ikatu et al., Bio/Technol. 8:241-242 (1990), the entirety of which is herein incorporated by reference); a tyrosinase gene (Katz et al., J. Gen. Microbiol. 129:2703-2714 (1983), the entirety of which is herein incorporated by reference) which encodes an enzyme capable of oxidizing tyrosine to DOPA and dopaquinone which in turn condenses to melanin; an α-galactosidase, which will turn a chromogenic α-galactose substrate.

Included within the terms “selectable or screenable marker genes” are also genes which encode a secretable marker whose secretion can be detected as a means of identifying or selecting for transformed cells. Examples include markers which encode a secretable antigen that can be identified by antibody interaction, or even secretable enzymes which can be detected catalytically. Secretable proteins fall into a number of classes, including small, diffusible proteins which are detectable, (e.g., by ELISA), small active enzymes which are detectable in extracellular solution (e.g., α-amylase, β-lactamase, phosphinothricin transferase), or proteins which are inserted or trapped in the cell wall (such as proteins which include a leader sequence such as that found in the expression unit of extension or tobacco PR-S). Other possible selectable and/or screenable marker genes will be apparent to those of skill in the art.

There are many methods for introducing transforming nucleic acid molecules into plant cells. Suitable methods are believed to include virtually any method by which nucleic acid molecules may be introduced into a cell, such as by Agrobacterium infection or direct delivery of nucleic acid molecules such as, for example, by PEG-mediated transformation, by electroporation or by acceleration of DNA coated particles, etc (Potrykus, Ann. Rev. Plant Physiol. Plant Mol. Biol. 42:205-225 (1991), the entirety of which is herein incorporated by reference; Vasil, Plant Mol. Biol. 25:925-937 (1994), the entirety of which is herein incorporated by reference). For example, electroporation has been used to transform maize protoplasts (Fromm et al., Nature 312:791-793 (1986), the entirety of which is herein incorporated by reference).

Other vector systems suitable for introducing transforming DNA into a host plant cell include but are not limited to binary artificial chromosome (BIBAC) vectors (Hamilton et al., Gene 200:107-116 (1997), the entirety of which is herein incorporated by reference); and transfection with RNA viral vectors (Della-Cioppa et al., Ann. N.Y. Acad. Sci. (1996), 792 (Engineering Plants for Commercial Products and Applications), 57-61, the entirety of which is herein incorporated by reference). Additional vector systems also include plant selectable YAC vectors such as those described in Mullen et al., Molecular Breeding 4:449-457 (1988), the entirety of which is herein incorporated by reference).

Technology for introduction of DNA into cells is well known to those of skill in the art. Four general methods for delivering a gene into cells have been described: (1) chemical methods (Graham and van der Eb, Virology 54:536-539 (1973), the entirety of which is herein incorporated by reference); (2) physical methods such as microinjection (Capecchi, Cell 22:479-488 (1980), the entirety of which is herein incorporated by reference), electroporation (Wong and Neumann, Biochem. Biophys. Res. Commun. 107:584-587 (1982); Fromm et al., Proc. Natl. Acad. Sci. (U.S.A.) 82:5824-5828 (1985); U.S. Pat. No. 5,384,253, all of which are herein incorporated in their entirety); and the gene gun (Johnston and Tang, Methods Cell Biol. 43:353-365 (1994), the entirety of which is herein incorporated by reference); (3) viral vectors (Clapp, Clin. Perinatol. 20:155-168 (1993); Lu et al., J. Exp. Med. 178:2089-2096 (1993); Eglitis and Anderson, Biotechniques 6:608-614 (1988), all of which are herein incorporated in their entirety); and (4) receptor-mediated mechanisms (Curiel et al., Hum. Gen. Ther. 3:147-154 (1992), Wagner et al., Proc. Natl. Acad. Sci. (USA) 89:6099-6103 (1992), both of which are incorporated by reference in their entirety).

Acceleration methods that may be used include, for example, microprojectile bombardment and the like. One example of a method for delivering transforming nucleic acid molecules to plant cells is microprojectile bombardment. This method has been reviewed by Yang and Christou (eds.), Particle Bombardment Technology for Gene Transfer, Oxford Press, Oxford, England (1994), the entirety of which is herein incorporated by reference). Non-biological particles (microprojectiles) that may be coated with nucleic acids and delivered into cells by a propelling force. Exemplary particles include those comprised of tungsten, gold, platinum and the like.

A particular advantage of microprojectile bombardment, in addition to it being an effective means of reproducibly transforming monocots, is that neither the isolation of protoplasts (Cristou et al., Plant Physiol. 87:671-674 (1988), the entirety of which is herein incorporated by reference) nor the susceptibility of Agrobacterium infection are required. An illustrative embodiment of a method for delivering DNA into maize cells by acceleration is a biolistics α-particle delivery system, which can be used to propel particles coated with DNA through a screen, such as a stainless steel or Nytex screen, onto a filter surface covered with corn cells cultured in suspension. Gordon-Kamm et al., describes the basic procedure for coating tungsten particles with DNA (Gordon-Kamm et al., Plant Cell 2:603-618 (1990), the entirety of which is herein incorporated by reference). The screen disperses the tungsten nucleic acid particles so that they are not delivered to the recipient cells in large aggregates. A particle delivery system suitable for use with the present invention is the helium acceleration PDS-1000/He gun is available from Bio-Rad Laboratories (Bio-Rad, Hercules, Calif.)(Sanford et al., Technique 3:3-16 (1991), the entirety of which is herein incorporated by reference).

For the bombardment, cells in suspension may be concentrated on filters. Filters containing the cells to be bombarded are positioned at an appropriate distance below the microprojectile stopping plate. If desired, one or more screens are also positioned between the gun and the cells to be bombarded.

Alternatively, immature embryos or other target cells may be arranged on solid culture medium. The cells to be bombarded are positioned at an appropriate distance below the microprojectile stopping plate. If desired, one or more screens are also positioned between the acceleration device and the cells to be bombarded. Through the use of techniques set forth herein one may obtain up to 1000 or more foci of cells transiently expressing a marker gene. The number of cells in a focus which express the exogenous gene product 48 hours post-bombardment often range from one to ten and average one to three.

In bombardment transformation, one may optimize the pre-bombardment culturing conditions and the bombardment parameters to yield the maximum numbers of stable transformants. Both the physical and biological parameters for bombardment are important in this technology. Physical factors are those that involve manipulating the DNA/microprojectile precipitate or those that affect the flight and velocity of either the macro- or microprojectiles. Biological factors include all steps involved in manipulation of cells before and immediately after bombardment, the osmotic adjustment of target cells to help alleviate the trauma associated with bombardment and also the nature of the transforming DNA, such as linearized DNA or intact supercoiled plasmids. It is believed that pre-bombardment manipulations are especially important for successful transformation of immature embryos.

In another alternative embodiment, plastids can be stably transformed. Methods disclosed for plastid transformation in higher plants include the particle gun delivery of DNA containing a selectable marker and targeting of the DNA to the plastid genome through homologous recombination (Svab et al., Proc. Natl. Acad. Sci. (U.S.A.) 87:8526-8530 (1990); Svab and Maliga, Proc. Natl. Acad. Sci. (U.S.A.) 90:913-917 (1993); Staub and Maliga, EMBO J. 12:601-606 (1993); U.S. Pat. Nos. 5,451,513 and 5,545,818, all of which are herein incorporated by reference in their entirety).

Accordingly, it is contemplated that one may wish to adjust various aspects of the bombardment parameters in small scale studies to fully optimize the conditions. One may particularly wish to adjust physical parameters such as gap distance, flight distance, tissue distance and helium pressure. One may also minimize the trauma reduction factors by modifying conditions which influence the physiological state of the recipient cells and which may therefore influence transformation and integration efficiencies. For example, the osmotic state, tissue hydration and the subculture stage or cell cycle of the recipient cells may be adjusted for optimum transformation. The execution of other routine adjustments will be known to those of skill in the art in light of the present disclosure.

Agrobacterium-mediated transfer is a widely applicable system for introducing genes into plant cells because the DNA can be introduced into whole plant tissues, thereby bypassing the need for regeneration of an intact plant from a protoplast. The use of Agrobacterium-mediated plant integrating vectors to introduce DNA into plant cells is well known in the art. See, for example the methods described by Fraley et al., Bio/Technology 3:629-635 (1985) and Rogers et al., Methods Enzymol. 153:253-277 (1987), both of which are herein incorporated by reference in their entirety. Further, the integration of the Ti-DNA is a relatively precise process resulting in few rearrangements. The region of DNA to be transferred is defined by the border sequences and intervening DNA is usually inserted into the plant genome as described (Spielmann et al., Mol. Gen. Genet. 205:34 (1986), the entirety of which is herein incorporated by reference).

Modern Agrobacterium transformation vectors are capable of replication in E. coli as well as Agrobacterium, allowing for convenient manipulations as described (Klee et al., In: Plant DNA Infectious Agents, Hohn and Schell (eds.), Springer-Verlag, New York, pp. 179-203 (1985), the entirety of which is herein incorporated by reference. Moreover, technological advances in vectors for Agrobacterium-mediated gene transfer have improved the arrangement of genes and restriction sites in the vectors to facilitate construction of vectors capable of expressing various polypeptide coding genes. The vectors described have convenient multi-linker regions flanked by a promoter and a polyadenylation site for direct expression of inserted polypeptide coding genes and are suitable for present purposes (Rogers et al., Methods Enzymol. 153:253-277 (1987)). In addition, Agrobacterium containing both armed and disarmed Ti genes can be used for the transformations. In those plant strains where Agrobacterium-mediated transformation is efficient, it is the method of choice because of the facile and defined nature of the gene transfer.

A transgenic plant formed using Agrobacterium transformation methods typically contains a single gene on one chromosome. Such transgenic plants can be referred to as being heterozygous for the added gene. More preferred is a transgenic plant that is homozygous for the added structural gene; i.e., a transgenic plant that contains two added genes, one gene at the same locus on each chromosome of a chromosome pair. A homozygous transgenic plant can be obtained by sexually mating (selfing) an independent segregant transgenic plant that contains a single added gene, germinating some of the seed produced and analyzing the resulting plants produced for the gene of interest.

It is also to be understood that two different transgenic plants can also be mated to produce offspring that contain two independently segregating added, exogenous genes. Selfing of appropriate progeny can produce plants that are homozygous for both added, exogenous genes that encode a polypeptide of interest. Back-crossing to a parental plant and out-crossing with a non-transgenic plant are also contemplated, as is vegetative propagation.

Transformation of plant protoplasts can be achieved using methods based on calcium phosphate precipitation, polyethylene glycol treatment, electroporation and combinations of these treatments (See, for example, Potrykus et al., Mol. Gen. Genet. 205:193-200 (1986); Lorz et al., Mol. Gen. Genet. 199:178 (1985); Fromm et al., Nature 319:791 (1986); Uchimiya et al., Mol. Gen. Genet. 204:204 (1986); Marcotte et al., Nature 335:454-457 (1988), all of which are herein incorporated by reference in their entirety).

Application of these systems to different plant strains depends upon the ability to regenerate that particular plant strain from protoplasts. Illustrative methods for the regeneration of cereals from protoplasts are described (Fujimura et al., Plant Tissue Culture Letters 2:74 (1985); Toriyama et al., Theor Appl. Genet. 205:34 (1986); Yamada et al., Plant Cell Rep. 4:85 (1986); Abdullah et al., Biotechnology 4:1087 (1986), all of which are herein incorporated by reference in their entirety).

To transform plant strains that cannot be successfully regenerated from protoplasts, other ways to introduce DNA into intact cells or tissues can be utilized. For example, regeneration of cereals from immature embryos or explants can be effected as described (Vasil, Biotechnology 6:397 (1988), the entirety of which is herein incorporated by reference). In addition, “particle gun” or high-velocity microprojectile technology can be utilized (Vasil et al., Bio/Technology 10:667 (1992), the entirety of which is herein incorporated by reference).

Using the latter technology, DNA is carried through the cell wall and into the cytoplasm on the surface of small metal particles as described (Klein et al., Nature 328:70 (1987); Klein et al., Proc. Natl. Acad. Sci. (U.S.A.) 85:8502-8505 (1988); McCabe et al., Bio/Technology 6:923 (1988), all of which are herein incorporated by reference in their entirety). The metal particles penetrate through several layers of cells and thus allow the transformation of cells within tissue explants.

Other methods of cell transformation can also be used and include but are not limited to introduction of DNA into plants by direct DNA transfer into pollen (Zhou et al., Methods Enzymol. 101:433 (1983); Hess et al., Intern Rev. Cytol. 107:367 (1987); Luo et al., Plant Mol. Biol. Reporter 6:165 (1988), all of which are herein incorporated by reference in their entirety), by direct injection of DNA into reproductive organs of a plant (Pena et al., Nature 325:274 (1987), the entirety of which is herein incorporated by reference), or by direct injection of DNA into the cells of immature embryos followed by the rehydration of desiccated embryos (Neuhaus et al., Theor. Appl. Genet. 75:30 (1987), the entirety of which is herein incorporated by reference).

The regeneration, development and cultivation of plants from single plant protoplast transformants or from various transformed explants is well known in the art (Weissbach and Weissbach, In: Methods for Plant Molecular Biology, Academic Press, San Diego, Calif., (1988), the entirety of which is herein incorporated by reference). This regeneration and growth process typically includes the steps of selection of transformed cells, culturing those individualized cells through the usual stages of embryonic development through the rooted plantlet stage. Transgenic embryos and seeds are similarly regenerated. The resulting transgenic rooted shoots are thereafter planted in an appropriate plant growth medium such as soil.

The development or regeneration of plants containing the foreign, exogenous gene that encodes a protein of interest is well known in the art. Preferably, the regenerated plants are self-pollinated to provide homozygous transgenic plants. Otherwise, pollen obtained from the regenerated plants is crossed to seed-grown plants of agronomically important lines. Conversely, pollen from plants of these important lines is used to pollinate regenerated plants. A transgenic plant of the present invention containing a desired polypeptide is cultivated using methods well known to one skilled in the art.

There are a variety of methods for the regeneration of plants from plant tissue. The particular method of regeneration will depend on the starting plant tissue and the particular plant species to be regenerated.

Methods for transforming dicots, primarily by use of Agrobacterium tumefaciens and obtaining transgenic plants have been published for cotton (U.S. Pat. No. 5,004,863; U.S. Pat. No. 5,159,135; U.S. Pat. No. 5,518,908, all of which are herein incorporated by reference in their entirety); soybean (U.S. Pat. No. 5,569,834; U.S. Pat. No. 5,416,011; McCabe et. al., Biotechnology 6:923 (1988); Christou et al., Plant Physiol. 87:671-674 (1988); all of which are herein incorporated by reference in their entirety); Brassica (U.S. Pat. No. 5,463,174, the entirety of which is herein incorporated by reference); peanut (Cheng et al., Plant Cell Rep. 15:653-657 (1996), McKently et al., Plant Cell Rep. 14:699-703 (1995), all of which are herein incorporated by reference in their entirety); papaya; and pea (Grant et al., Plant Cell Rep. 15:254-258 (1995), the entirety of which is herein incorporated by reference).

Transformation of monocotyledons using electroporation, particle bombardment and Agrobacterium have also been reported. Transformation and plant regeneration have been achieved in asparagus (Bytebier et al., Proc. Natl. Acad. Sci. (USA) 84:5354 (1987), the entirety of which is herein incorporated by reference); barley (Wan and Lemaux, Plant Physiol 104:37 (1994), the entirety of which is herein incorporated by reference); maize (Rhodes et al., Science 240:204 (1988); Gordon-Kamm et al., Plant Cell 2:603-618 (1990); Fromm et al., Bio/Technology 8:833 (1990); Koziel et al., Bio/Technology 11:194 (1993); Armstrong et al., Crop Science 35:550-557 (1995); all of which are herein incorporated by reference in their entirety); oat (Somers et al., Bio/Technology 10:1589 (1992), the entirety of which is herein incorporated by reference); orchard grass (Horn et al., Plant Cell Rep. 7:469 (1988), the entirety of which is herein incorporated by reference); rice (Toriyama et al., Theor Appl. Genet. 205:34 (1986); Part et al., Plant Mol. Biol. 32:1135-1148 (1996); Abedinia et al., Aust. J. Plant Physiol. 24:133-141 (1997); Zhang and Wu, Theor. Appl. Genet. 76:835 (1988); Zhang et al., Plant Cell Rep. 7:379 (1988); Battraw and Hall, Plant Sci. 86:191-202 (1992); Christou et al., Bio/Technology 9:957 (1991), all of which are herein incorporated by reference in their entirety); rye (De la Pena et al., Nature 325:274 (1987), the entirety of which is herein incorporated by reference); sugarcane (Bower and Birch, Plant J. 2:409 (1992), the entirety of which is herein incorporated by reference); tall fescue (Wang et al., Bio/Technology 10:691 (1992), the entirety of which is herein incorporated by reference) and wheat (Vasil et al., Bio/Technology 10:667 (1992), the entirety of which is herein incorporated by reference; U.S. Pat. No. 5,631,152, the entirety of which is herein incorporated by reference).

Assays for gene expression based on the transient expression of cloned nucleic acid constructs have been developed by introducing the nucleic acid molecules into plant cells by polyethylene glycol treatment, electroporation, or particle bombardment (Marcotte et al., Nature 335:454-457 (1988), the entirety of which is herein incorporated by reference; Marcotte et al., Plant Cell 1:523-532 (1989), the entirety of which is herein incorporated by reference; McCarty et al., Cell 66:895-905 (1991), the entirety of which is herein incorporated by reference; Hattori et al., Genes Dev. 6:609-618 (1992), the entirety of which is herein incorporated by reference; Goff et al., EMBO J. 9:2517-2522 (1990), the entirety of which is herein incorporated by reference). Transient expression systems may be used to functionally dissect gene constructs (see generally, Mailga et al., Methods in Plant Molecular Biology, Cold Spring Harbor Press (1995)).

Any of the nucleic acid molecules of the present invention may be introduced into a plant cell in a permanent or transient manner in combination with other genetic elements such as vectors, promoters, enhancers etc. Further, any of the nucleic acid molecules of the present invention may be introduced into a plant cell in a manner that allows for overexpression of the protein or fragment thereof encoded by the nucleic acid molecule.

Cosuppression is the reduction in expression levels, usually at the level of RNA, of a particular endogenous gene or gene family by the expression of a homologous sense construct that is capable of transcribing mRNA of the same strandedness as the transcript of the endogenous gene (Napoli et al., Plant Cell 2:279-289 (1990), the entirety of which is herein incorporated by reference; van der Krol et al., Plant Cell 2:291-299 (1990), the entirety of which is herein incorporated by reference). Cosuppression may result from stable transformation with a single copy nucleic acid molecule that is homologous to a nucleic acid sequence found with the cell (Prolls and Meyer, Plant J. 2:465-475 (1992), the entirety of which is herein incorporated by reference) or with multiple copies of a nucleic acid molecule that is homologous to a nucleic acid sequence found with the cell (Mittlesten et al, Mol. Gen. Genet. 244:325-330 (1994), the entirety of which is herein incorporated by reference). Genes, even though different, linked to homologous promoters may result in the cosuppression of the linked genes (Vaucheret, C. R. Acad. Sci. III 316:1471-1483 (1993), the entirety of which is herein incorporated by reference).

This technique has, for example, been applied to generate white flowers from red petunia and tomatoes that do not ripen on the vine. Up to 50% of petunia transformants that contained a sense copy of the glucoamylase (CHS) gene produced white flowers or floral sectors; this was as a result of the post-transcriptional loss of mRNA encoding CHS (Flavell, Proc. Natl. Acad. Sci. (U.S.A.) 91:3490-3496 (1994), the entirety of which is herein incorporated by reference); van Blokland et al., Plant J. 6:861-877 (1994), the entirety of which is herein incorporated by reference). Cosuppression may require the coordinate transcription of the transgene and the endogenous gene and can be reset by a developmental control mechanism (Jorgensen, Trends Biotechnol. 8:340-344 (1990), the entirety of which is herein incorporated by reference; Meins and Kunz, In: Gene Inactivation and Homologous Recombination in Plants, Paszkowski (ed.), pp. 335-348, Kluwer Academic, Netherlands (1994), the entirety of which is herein incorporated by reference).

It is understood that one or more of the nucleic acids of the present invention may be introduced into a plant cell and transcribed using an appropriate promoter with such transcription resulting in the cosuppression of an endogenous carbon assimilation pathway enzyme.

Antisense approaches are a way of preventing or reducing gene function by targeting the genetic material (Mol et al., FEBS Lett. 268:427-430 (1990), the entirety of which is herein incorporated by reference). The objective of the antisense approach is to use a sequence complementary to the target gene to block its expression and create a mutant cell line or organism in which the level of a single chosen protein is selectively reduced or abolished. Antisense techniques have several advantages over other ‘reverse genetic’ approaches. The site of inactivation and its developmental effect can be manipulated by the choice of promoter for antisense genes or by the timing of external application or microinjection. Antisense can manipulate its specificity by selecting either unique regions of the target gene or regions where it shares homology to other related genes (Hiatt et al., In: Genetic Engineering, Setlow (ed.), Vol. 11, New York: Plenum 49-63 (1989), the entirety of which is herein incorporated by reference).

The principle of regulation by antisense RNA is that RNA that is complementary to the target mRNA is introduced into cells, resulting in specific RNA:RNA duplexes being formed by base pairing between the antisense substrate and the target mRNA (Green et al., Annu. Rev. Biochem. 55:569-597 (1986), the entirety of which is herein incorporated by reference). Under one embodiment, the process involves the introduction and expression of an antisense gene sequence. Such a sequence is one in which part or all of the normal gene sequences are placed under a promoter in inverted orientation so that the ‘wrong’ or complementary strand is transcribed into a noncoding antisense RNA that hybridizes with the target mRNA and interferes with its expression (Takayama and Inouye, Crit. Rev. Biochem. Mol. Biol. 25:155-184 (1990), the entirety of which is herein incorporated by reference). An antisense vector is constructed by standard procedures and introduced into cells by transformation, transfection, electroporation, microinjection, infection, etc. The type of transformation and choice of vector will determine whether expression is transient or stable. The promoter used for the antisense gene may influence the level, timing, tissue, specificity, or inducibility of the antisense inhibition.

It is understood that the activity of a carbon assimilation pathway enzyme in a plant cell may be reduced or depressed by growing a transformed plant cell containing a nucleic acid molecule whose non-transcribed strand encodes a carbon assimilation pathway enzyme or fragment thereof.

Antibodies have been expressed in plants (Hiatt et al., Nature 342:76-78 (1989), the entirety of which is herein incorporated by reference; Conrad and Fielder, Plant Mol. Biol. 26:1023-1030 (1994), the entirety of which is herein incorporated by reference). Cytoplasmic expression of a scFv (single-chain Fv antibodies) has been reported to delay infection by artichoke mottled crinkle virus. Transgenic plants that express antibodies directed against endogenous proteins may exhibit a physiological effect (Philips et al., EMBO J. 16:4489-4496 (1997), the entirety of which is herein incorporated by reference; Marion-Poll, Trends in Plant Science 2:447-448 (1997), the entirety of which is herein incorporated by reference). For example, expressed anti-abscisic antibodies have been reported to result in a general perturbation of seed development (Philips et al., EMBO J. 16: 4489-4496 (1997)).

Antibodies that are catalytic may also be expressed in plants (abzymes). The principle behind abzymes is that since antibodies may be raised against many molecules, this recognition ability can be directed toward generating antibodies that bind transition states to force a chemical reaction forward (Persidas, Nature Biotechnology 15:1313-1315 (1997), the entirety of which is herein incorporated by reference; Baca et al., Ann. Rev. Biophys. Biomol. Struct. 26:461-493 (1997), the entirety of which is herein incorporated by reference). The catalytic abilities of abzymes may be enhanced by site directed mutagenesis. Examples of abzymes are, for example, set forth in U.S. Pat. No. 5,658,753; U.S. Pat. No. 5,632,990; U.S. Pat. No. 5,631,137; U.S. Pat. No. 5,602,015; U.S. Pat. No. 5,559,538; U.S. Pat. No. 5,576,174; U.S. Pat. No. 5,500,358; U.S. Pat. No. 5,318,897; U.S. Pat. No. 5,298,409; U.S. Pat. No. 5,258,289 and U.S. Pat. No. 5,194,585, all of which are herein incorporated in their entirety.

It is understood that any of the antibodies of the present invention may be expressed in plants and that such expression can result in a physiological effect. It is also understood that any of the expressed antibodies may be catalytic.

(b) Fungal Constructs and Fungal Transformants

The present invention also relates to a fungal recombinant vector comprising exogenous genetic material. The present invention also relates to a fungal cell comprising a fungal recombinant vector. The present invention also relates to methods for obtaining a recombinant fungal host cell comprising introducing into a fungal host cell exogenous genetic material.

Exogenous genetic material may be transferred into a fungal cell. In a preferred embodiment the exogenous genetic material includes a nucleic acid molecule of the present invention having a sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341 or complements thereof or fragments of either or other nucleic acid molecule of the present invention. The fungal recombinant vector may be any vector which can be conveniently subjected to recombinant DNA procedures. The choice of a vector will typically depend on the compatibility of the vector with the fungal host cell into which the vector is to be introduced. The vector may be a linear or a closed circular plasmid. The vector system may be a single vector or plasmid or two or more vectors or plasmids which together contain the total DNA to be introduced into the genome of the fungal host.

The fungal vector may be an autonomously replicating vector, i.e., a vector which exists as an extrachromosomal entity, the replication of which is independent of chromosomal replication, e.g., a plasmid, an extrachromosomal element, a minichromosome, or an artificial chromosome. The vector may contain any means for assuring self-replication. Alternatively, the vector may be one which, when introduced into the fungal cell, is integrated into the genome and replicated together with the chromosome(s) into which it has been integrated. For integration, the vector may rely on the nucleic acid sequence of the vector for stable integration of the vector into the genome by homologous or nonhomologous recombination. Alternatively, the vector may contain additional nucleic acid sequences for directing integration by homologous recombination into the genome of the fungal host. The additional nucleic acid sequences enable the vector to be integrated into the host cell genome at a precise location(s) in the chromosome(s). To increase the likelihood of integration at a precise location, there should be preferably two nucleic acid sequences which individually contain a sufficient number of nucleic acids, preferably 400 bp to 1500 bp, more preferably 800 bp to 1000 bp, which are highly homologous with the corresponding target sequence to enhance the probability of homologous recombination. These nucleic acid sequences may be any sequence that is homologous with a target sequence in the genome of the fungal host cell and, furthermore, may be non-encoding or encoding sequences.

For autonomous replication, the vector may further comprise an origin of replication enabling the vector to replicate autonomously in the host cell in question. Examples of origin of replications for use in a yeast host cell are the 2 micron origin of replication and the combination of CEN3 and ARS 1. Any origin of replication may be used which is compatible with the fungal host cell of choice.

The fungal vectors of the present invention preferably contain one or more selectable markers which permit easy selection of transformed cells. A selectable marker is a gene the product of which provides, for example biocide or viral resistance, resistance to heavy metals, prototrophy to auxotrophs and the like. The selectable marker may be selected from the group including, but not limited to, amdS (acetamidase), argB (ornithine carbamoyltransferase), bar (phosphinothricin acetyltransferase), hygB (hygromycin phosphotransferase), niaD (nitrate reductase), pyrG (orotidine-5′-phosphate decarboxylase) and sC (sulfate adenyltransferase) and trpC (anthranilate synthase). Preferred for use in an Aspergillus cell are the amdS and pyrG markers of Aspergillus nidulans or Aspergillus oryzae and the bar marker of Streptomyces hygroscopicus. Furthermore, selection may be accomplished by co-transformation, e.g., as described in WO 91/17243, the entirety of which is herein incorporated by reference. A nucleic acid sequence of the present invention may be operably linked to a suitable promoter sequence. The promoter sequence is a nucleic acid sequence which is recognized by the fungal host cell for expression of the nucleic acid sequence. The promoter sequence contains transcription and translation control sequences which mediate the expression of the protein or fragment thereof.

A promoter may be any nucleic acid sequence which shows transcriptional activity in the fungal host cell of choice and may be obtained from genes encoding polypeptides either homologous or heterologous to the host cell. Examples of suitable promoters for directing the transcription of a nucleic acid construct of the invention in a filamentous fungal host are promoters obtained from the genes encoding Aspergillus oryzae TAKA amylase, Rhizomucor miehei aspartic proteinase, Aspergillus niger neutral alpha-amylase, Aspergillus niger acid stable alpha-amylase, Aspergillus niger or Aspergillus awamori glucoamylase (glaA), Rhizomucor miehei lipase, Aspergillus oryzae alkaline protease, Aspergillus oryzae triose phosphate isomerase, Aspergillus nidulans acetamidase and hybrids thereof. In a yeast host, a useful promoter is the Saccharomyces cerevisiae enolase (eno-1) promoter. Particularly preferred promoters are the TAKA amylase, NA2-tpi (a hybrid of the promoters from the genes encoding Aspergillus niger neutral alpha-amylase and Aspergillus oryzae triose phosphate isomerase) and glaA promoters.

A protein or fragment thereof encoding nucleic acid molecule of the present invention may also be operably linked to a terminator sequence at its 3′ terminus. The terminator sequence may be native to the nucleic acid sequence encoding the protein or fragment thereof or may be obtained from foreign sources. Any terminator which is functional in the fungal host cell of choice may be used in the present invention, but particularly preferred terminators are obtained from the genes encoding Aspergillus oryzae TAKA amylase, Aspergillus niger glucoamylase, Aspergillus nidulans anthranilate synthase, Aspergillus niger alpha-glucosidase and Saccharomyces cerevisiae enolase.

A protein or fragment thereof encoding nucleic acid molecule of the present invention may also be operably linked to a suitable leader sequence. A leader sequence is a nontranslated region of a mRNA which is important for translation by the fungal host. The leader sequence is operably linked to the 5′ terminus of the nucleic acid sequence encoding the protein or fragment thereof. The leader sequence may be native to the nucleic acid sequence encoding the protein or fragment thereof or may be obtained from foreign sources. Any leader sequence which is functional in the fungal host cell of choice may be used in the present invention, but particularly preferred leaders are obtained from the genes encoding Aspergillus oryzae TAKA amylase and Aspergillus oryzae triose phosphate isomerase.

A polyadenylation sequence may also be operably linked to the 3′ terminus of the nucleic acid sequence of the present invention. The polyadenylation sequence is a sequence which when transcribed is recognized by the fungal host to add polyadenosine residues to transcribed mRNA. The polyadenylation sequence may be native to the nucleic acid sequence encoding the protein or fragment thereof or may be obtained from foreign sources. Any polyadenylation sequence which is functional in the fungal host of choice may be used in the present invention, but particularly preferred polyadenylation sequences are obtained from the genes encoding Aspergillus oryzae TAKA amylase, Aspergillus niger glucoamylase, Aspergillus nidulans anthranilate synthase and Aspergillus niger alpha-glucosidase.

To avoid the necessity of disrupting the cell to obtain the protein or fragment thereof and to minimize the amount of possible degradation of the expressed protein or fragment thereof within the cell, it is preferred that expression of the protein or fragment thereof gives rise to a product secreted outside the cell. To this end, a protein or fragment thereof of the present invention may be linked to a signal peptide linked to the amino terminus of the protein or fragment thereof. A signal peptide is an amino acid sequence which permits the secretion of the protein or fragment thereof from the fungal host into the culture medium. The signal peptide may be native to the protein or fragment thereof of the invention or may be obtained from foreign sources. The 5′ end of the coding sequence of the nucleic acid sequence of the present invention may inherently contain a signal peptide coding region naturally linked in translation reading frame with the segment of the coding region which encodes the secreted protein or fragment thereof. Alternatively, the 5′ end of the coding sequence may contain a signal peptide coding region which is foreign to that portion of the coding sequence which encodes the secreted protein or fragment thereof. The foreign signal peptide may be required where the coding sequence does not normally contain a signal peptide coding region. Alternatively, the foreign signal peptide may simply replace the natural signal peptide to obtain enhanced secretion of the desired protein or fragment thereof. The foreign signal peptide coding region may be obtained from a glucoamylase or an amylase gene from an Aspergillus species, a lipase or proteinase gene from Rhizomucor miehei, the gene for the alpha-factor from Saccharomyces cerevisiae, or the calf preprochymosin gene. An effective signal peptide for fungal host cells is the Aspergillus oryzae TAKA amylase signal, Aspergillus niger neutral amylase signal, the Rhizomucor miehei aspartic proteinase signal, the Humicola lanuginosus cellulase signal, or the Rhizomucor miehei lipase signal. However, any signal peptide capable of permitting secretion of the protein or fragment thereof in a fungal host of choice may be used in the present invention.

A protein or fragment thereof encoding nucleic acid molecule of the present invention may also be linked to a propeptide coding region. A propeptide is an amino acid sequence found at the amino terminus of a proprotein or proenzyme. Cleavage of the propeptide from the proprotein yields a mature biochemically active protein. The resulting polypeptide is known as a propolypeptide or proenzyme (or a zymogen in some cases). Propolypeptides are generally inactive and can be converted to mature active polypeptides by catalytic or autocatalytic cleavage of the propeptide from the propolypeptide or proenzyme. The propeptide coding region may be native to the protein or fragment thereof or may be obtained from foreign sources. The foreign propeptide coding region may be obtained from the Saccharomyces cerevisiae alpha-factor gene or Myceliophthora thermophila laccase gene (WO 95/33836, the entirety of which is herein incorporated by reference).

The procedures used to ligate the elements described above to construct the recombinant expression vector of the present invention are well known to one skilled in the art (see, for example, Sambrook et al., Molecular Cloning, A Laboratory Manual, 2nd ed., Cold Spring Harbor, N.Y., (1989)).

The present invention also relates to recombinant fungal host cells produced by the methods of the present invention which are advantageously used with the recombinant vector of the present invention. The cell is preferably transformed with a vector comprising a nucleic acid sequence of the invention followed by integration of the vector into the host chromosome. The choice of fungal host cells will to a large extent depend upon the gene encoding the protein or fragment thereof and its source. The fungal host cell may, for example, be a yeast cell or a filamentous fungal cell.

“Yeast” as used herein includes Ascosporogenous yeast (Endomycetales), Basidiosporogenous yeast and yeast belonging to the Fungi Imperfecti (Blastomycetes). The Ascosporogenous yeasts are divided into the families Spermophthoraceae and Saccharomycetaceae. The latter is comprised of four subfamilies, Schizosaccharomycoideae (for example, genus Schizosaccharomyces), Nadsonioideae, Lipomycoideae and Saccharomycoideae (for example, genera Pichia, Kluyveromyces and Saccharomyces). The Basidiosporogenous yeasts include the genera Leucosporidim, Rhodosporidium, Sporidiobolus, Filobasidium and Filobasidiella. Yeast belonging to the Fungi Imperfecti are divided into two families, Sporobolomycetaceae (for example, genera Sorobolomyces and Bullera) and Cryptococcaceae (for example, genus Candida). Since the classification of yeast may change in the future, for the purposes of this invention, yeast shall be defined as described in Biology and Activities of Yeast (Skinner et al., Soc. App. Bacteriol. Symposium Series No. 9, (1980), the entirety of which is herein incorporated by reference). The biology of yeast and manipulation of yeast genetics are well known in the art (see, for example, Biochemistry and Genetics of Yeast, Bacil et al. (ed.), 2nd edition, 1987; The Yeasts, Rose and Harrison (eds.), 2nd ed., (1987); and The Molecular Biology of the Yeast Saccharomyces, Strathem et al. (eds.), (1981), all of which are herein incorporated by reference in their entirety).

“Fungi” as used herein includes the phyla Ascomycota, Basidiomycota, Chytridiomycota and Zygomycota (as defined by Hawksworth et al., In: Ainsworth and Bisby's Dictionary of The Fungi, 8th edition, 1995, CAB International, University Press, Cambridge, UK; the entirety of which is herein incorporated by reference) as well as the Oomycota (as cited in Hawksworth et al., In: Ainsworth and Bisby's Dictionary of The Fungi, 8th edition, 1995, CAB International, University Press, Cambridge, UK) and all mitosporic fingi (Hawksworth et al., In: Ainsworth and Bisby's Dictionary of The Fungi, 8th edition, 1995, CAB International, University Press, Cambridge, UK). Representative groups of Ascomycota include, for example, Neurospora, Eupenicillium (=Penicillium), Emericella (=Aspergillus), Eurotiun (=Aspergillus) and the true yeasts listed above. Examples of Basidiomycota include mushrooms, rusts and smuts. Representative groups of Chytridiomycota include, for example, Allomyces, Blastocladiella, Coelomomyces and aquatic fungi. Representative groups of Oomycota include, for example, Saprolegniomycetous aquatic fungi (water molds) such as Achlya. Examples of mitosporic fungi include Aspergillus, Penicilliun, Candida and Alternaria. Representative groups of Zygomycota include, for example, Rhizopus and Mucor.

“Filamentous fungi” include all filamentous forms of the subdivision Eumycota and Oomycota (as defined by Hawksworth et al., In: Ainsworth and Bisby's Dictionary of The Fungi, 8th edition, 1995, CAB International, University Press, Cambridge, UK). The filamentous fungi are characterized by a vegetative mycelium composed of chitin, cellulose, glucan, chitosan, mannan and other complex polysaccharides. Vegetative growth is by hyphal elongation and carbon catabolism is obligately aerobic. In contrast, vegetative growth by yeasts such as Saccharomyces cerevisiae is by budding of a unicellular thallus and carbon catabolism may be fermentative.

In one embodiment, the fungal host cell is a yeast cell. In a preferred embodiment, the yeast host cell is a cell of the species of Candida, Kluyveromyces, Saccharomyces, Schizosaccharomyces, Pichia and Yarrowia. In a preferred embodiment, the yeast host cell is a Saccharomyces cerevisiae cell, a Saccharomyces carisbergensis, Saccharomyces diastaticus cell, a Saccharomyces douglasii cell, a Saccharomyces kluyveri cell, a Saccharomyces norbensis cell, or a Saccharomyces oviformis cell. In another preferred embodiment, the yeast host cell is a Kluyveromyces lactis cell. In another preferred embodiment, the yeast host cell is a Yarrowia lipolytica cell.

In another embodiment, the fungal host cell is a filamentous fungal cell. In a preferred embodiment, the filamentous fungal host cell is a cell of the species of, but not limited to, Acremonium, Aspergillus, Fusarium, Humicola, Myceliophthora, Mucor, Neurospora, Penicillium, Thielavia, Tolypocladium and Trichoderma. In a preferred embodiment, the filamentous fungal host cell is an Aspergillus cell. In another preferred embodiment, the filamentous fungal host cell is an Acremonium cell. In another preferred embodiment, the filamentous fungal host cell is a Fusarium cell. In another preferred embodiment, the filamentous fungal host cell is a Humicola cell. In another preferred embodiment, the filamentous fungal host cell is a Myceliophthora cell. In another even preferred embodiment, the filamentous fungal host cell is a Mucor cell. In another preferred embodiment, the filamentous fungal host cell is a Neurospora cell. In another preferred embodiment, the filamentous fungal host cell is a Penicillium cell. In another preferred embodiment, the filamentous fungal host cell is a Thielavia cell. In another preferred embodiment, the filamentous fungal host cell is a Tolypocladiun cell. In another preferred embodiment, the filamentous fungal host cell is a Trichoderma cell. In a preferred embodiment, the filamentous fungal host cell is an Aspergillus oryzae cell, an Aspergillus niger cell, an Aspergillus foetidus cell, or an Aspergillus japonicus cell. In another preferred embodiment, the filamentous fungal host cell is a Fusarium oxysporum cell or a Fusarium graminearum cell. In another preferred embodiment, the filamentous fungal host cell is a Humicola insolens cell or a Humicola lanuginosus cell. In another preferred embodiment, the filamentous fungal host cell is a Myceliophthora thermophila cell. In a most preferred embodiment, the filamentous fungal host cell is a Mucor miehei cell. In a most preferred embodiment, the filamentous fungal host cell is a Neurospora crassa cell. In a most preferred embodiment, the filamentous fungal host cell is a Penicillium purpurogenum cell. In another most preferred embodiment, the filamentous fungal host cell is a Thielavia terrestris cell. In another most preferred embodiment, the Trichoderma cell is a Trichoderma reesei cell, a Trichoderma viride cell, a Trichoderma longibrachiatum cell, a Trichoderma harzianum cell, or a Trichoderma koningii cell. In a preferred embodiment, the fungal host cell is selected from an A. nidulans cell, an A. niger cell, an A. oryzae cell and an A. sojae cell. In a further preferred embodiment, the fungal host cell is an A. nidulans cell.

The recombinant fungal host cells of the present invention may further comprise one or more sequences which encode one or more factors that are advantageous in the expression of the protein or fragment thereof, for example, an activator (e.g., a trans-acting factor), a chaperone and a processing protease. The nucleic acids encoding one or more of these factors are preferably not operably linked to the nucleic acid encoding the protein or fragment thereof. An activator is a protein which activates transcription of a nucleic acid sequence encoding a polypeptide (Kudla et al., EMBO 9:1355-1364 (1990); Jarai and Buxton, Current Genetics 26:2238-244 (1994); Verdier, Yeast 6:271-297 (1990), all of which are herein incorporated by reference in their entirety). The nucleic acid sequence encoding an activator may be obtained from the genes encoding Saccharomyces cerevisiae heme activator protein 1 (hap1), Saccharomyces cerevisiae galactose metabolizing protein 4 (gal4) and Aspergillus nidulans ammonia regulation protein (areA). For further examples, see Verdier, Yeast 6:271-297 (1990); MacKenzie et al., Journal of Gen. Microbiol. 139:2295-2307 (1993), both of which are herein incorporated by reference in their entirety). A chaperone is a protein which assists another protein in folding properly (Hartl et al., TIBS 19:20-25 (1994); Bergeron et al., TIBS 19:124-128 (1994); Demolder et al., J. Biotechnology 32:179-189 (1994); Craig, Science 260:1902-1903 (1993); Gething and Sambrook, Nature 355:33-45 (1992); Puig and Gilbert, J. Biol. Chem. 269:7764-7771 (1994); Wang and Tsou, FASEB Journal 7:1515-11157 (1993); Robinson et al., Bio/Technology 1:381-384 (1994), all of which are herein incorporated by reference in their entirety). The nucleic acid sequence encoding a chaperone may be obtained from the genes encoding Aspergillus oryzae protein disulphide isomerase, Saccharomyces cerevisiae calnexin, Saccharomyces cerevisiae BiP/GRP78 and Saccharomyces cerevisiae Hsp70. For further examples, see Gething and Sambrook, Nature 355:33-45 (1992); Hartl et al., TIBS 19:20-25 (1994). A processing protease is a protease that cleaves a propeptide to generate a mature biochemically active polypeptide (Enderlin and Ogrydziak, Yeast 10:67-79 (1994); Fuller et al., Proc. Natl. Acad. Sci. (U.S.A.) 86:1434-1438 (1989); Julius et al., Cell 37:1075-1089 (1984); Julius et al., Cell 32:839-852 (1983), all of which are incorporated by reference in their entirety). The nucleic acid sequence encoding a processing protease may be obtained from the genes encoding Aspergillus niger Kex2, Saccharomyces cerevisiae dipeptidylaminopeptidase, Saccharomyces cerevisiae Kex2 and Yarrowia lipolytica dibasic processing endoprotease (xpr6). Any factor that is functional in the fungal host cell of choice may be used in the present invention.

Fungal cells may be transformed by a process involving protoplast formation, transformation of the protoplasts and regeneration of the cell wall in a manner known per se. Suitable procedures for transformation of Aspergillus host cells are described in EP 238 023 and Yelton et al., Proc. Natl. Acad. Sci. (U.S.A.) 81:1470-1474 (1984), both of which are herein incorporated by reference in their entirety. A suitable method of transforming Fusarium species is described by Malardier et al., Gene 78:147-156 (1989), the entirety of which is herein incorporated by reference. Yeast may be transformed using the procedures described by Becker and Guarente, In: Abelson and Simon, (eds.), Guide to Yeast Genetics and Molecular Biology, Methods Enzymol. Volume 194, pp 182-187, Academic Press, Inc., New York; Ito et al., J. Bacteriology 153:163 (1983); Hinnen et al., Proc. Natl. Acad. Sci. (U.S.A.) 75:1920 (1978), all of which are herein incorporated by reference in their entirety.

The present invention also relates to methods of producing the protein or fragment thereof comprising culturing the recombinant fungal host cells under conditions conducive for expression of the protein or fragment thereof. The fungal cells of the present invention are cultivated in a nutrient medium suitable for production of the protein or fragment thereof using methods known in the art. For example, the cell may be cultivated by shake flask cultivation, small-scale or large-scale fermentation (including continuous, batch, fed-batch, or solid state fermentations) in laboratory or industrial fermentors performed in a suitable medium and under conditions allowing the protein or fragment thereof to be expressed and/or isolated. The cultivation takes place in a suitable nutrient medium comprising carbon and nitrogen sources and inorganic salts, using procedures known in the art (see, e.g., Bennett and LaSure (eds.), More Gene Manipulations in Fungi, Academic Press, CA, (1991), the entirety of which is herein incorporated by reference). Suitable media are available from commercial suppliers or may be prepared according to published compositions (e.g., in catalogues of the American Type Culture Collection, Manassas, Va.). If the protein or fragment thereof is secreted into the nutrient medium, a protein or fragment thereof can be recovered directly from the medium. If the protein or fragment thereof is not secreted, it is recovered from cell lysates.

The expressed protein or fragment thereof may be detected using methods known in the art that are specific for the particular protein or fragment. These detection methods may include the use of specific antibodies, formation of an enzyme product, or disappearance of an enzyme substrate. For example, if the protein or fragment thereof has enzymatic activity, an enzyme assay may be used. Alternatively, if polyclonal or monoclonal antibodies specific to the protein or fragment thereof are available, immunoassays may be employed using the antibodies to the protein or fragment thereof. The techniques of enzyme assay and immunoassay are well known to those skilled in the art.

The resulting protein or fragment thereof may be recovered by methods known in the arts. For example, the protein or fragment thereof may be recovered from the nutrient medium by conventional procedures including, but not limited to, centrifugation, filtration, extraction, spray-drying, evaporation, or precipitation. The recovered protein or fragment thereof may then be further purified by a variety of chromatographic procedures, e.g., ion exchange chromatography, gel filtration chromatography, affinity chromatography, or the like.

(c) Mammalian Constructs and Transformed Mammalian Cells

The present invention also relates to methods for obtaining a recombinant mammalian host cell, comprising introducing into a mammalian host cell exogenous genetic material. The present invention also relates to a mammalian cell comprising a mammalian recombinant vector. The present invention also relates to methods for obtaining a recombinant mammalian host cell, comprising introducing into a mammalian cell exogenous genetic material. In a preferred embodiment the exogenous genetic material includes a nucleic acid molecule of the present invention having a sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341 or complements thereof or fragments of either or other nucleic acid molecule of the present invention.

Mammalian cell lines available as hosts for expression are known in the art and include many immortalized cell lines available from the American Type Culture Collection (ATCC, Manassas, Va.), such as HeLa cells, Chinese hamster ovary (CHO) cells, baby hamster kidney (BHK) cells and a number of other cell lines. Suitable promoters for mammalian cells are also known in the art and include viral promoters such as that from Simian, Virus 40 (SV40) (Fiers et al., Nature 273:113 (1978), the entirety of which is herein incorporated by reference), Rous sarcoma virus (RSV), adenovirus (ADV) and bovine papilloma virus (BPV). Mammalian cells may also require terminator sequences and poly-A addition sequences. Enhancer sequences which increase expression may also be included and sequences which promote amplification of the gene may also be desirable (for example methotrexate resistance genes).

Vectors suitable for replication in mammalian cells may include viral replicons, or sequences which insure integration of the appropriate sequences encoding HCV epitopes into the host genome. For example, another vector used to express foreign DNA is vaccinia virus. In this case, for example, a nucleic acid molecule encoding a protein or fragment thereof is inserted into the vaccinia genome. Techniques for the insertion of foreign DNA into the vaccinia virus genome are known in the art and may utilize, for example, homologous recombination. Such heterologous DNA is generally inserted into a gene which is non-essential to the virus, for example, the thymidine kinase gene (tk), which also provides a selectable marker. Plasmid vectors that greatly facilitate the construction of recombinant viruses have been described (see, for example, Mackett et al, J Virol. 49:857 (1984); Chakrabarti et al., Mol. Cell. Biol. 5:3403 (1985); Moss, In: Gene Transfer Vectors For Mammalian Cells (Miller and Calos, eds., Cold Spring Harbor Laboratory, N.Y., p. 10, (1987); all of which are herein incorporated by reference in their entirety). Expression of the HCV polypeptide then occurs in cells or animals which are infected with the live recombinant vaccinia virus.

The sequence to be integrated into the mammalian sequence may be introduced into the primary host by any convenient means, which includes calcium precipitated DNA, spheroplast fusion, transformation, electroporation, biolistics, lipofection, microinjection, or other convenient means. Where an amplifiable gene is being employed, the amplifiable gene may serve as the selection marker for selecting hosts into which the amplifiable gene has been introduced. Alternatively, one may include with the amplifiable gene another marker, such as a drug resistance marker, e.g. neomycin resistance (G418 in mammalian cells), hygromycin in resistance etc., or an auxotrophy marker (HIS3, TRP1, LEU2, URA3, ADE2, LYS2, etc.) for use in yeast cells.

Depending upon the nature of the modification and associated targeting construct, various techniques may be employed for identifying targeted integration. Conveniently, the DNA may be digested with one or more restriction enzymes and the fragments probed with an appropriate DNA fragment which will identify the properly sized restriction fragment associated with integration.

One may use different promoter sequences, enhancer sequences, or other sequence which will allow for enhanced levels of expression in the expression host. Thus, one may combine an enhancer from one source, a promoter region from another source, a 5′-noncoding region upstream from the initiation methionine from the same or different source as the other sequences and the like. One may provide for an intron in the non-coding region with appropriate splice sites or for an alternative 3′-untranslated sequence or polyadenylation site. Depending upon the particular purpose of the modification, any of these sequences may be introduced, as desired.

Where selection is intended, the sequence to be integrated will have with it a marker gene, which allows for selection. The marker gene may conveniently be downstream from the target gene and may include resistance to a cytotoxic agent, e.g. antibiotics, heavy metals, or the like, resistance or susceptibility to HAT, gancyclovir, etc., complementation to an auxotrophic host, particularly by using an auxotrophic yeast as the host for the subject manipulations, or the like. The marker gene may also be on a separate DNA molecule, particularly with primary mammalian cells. Alternatively, one may screen the various transformants, due to the high efficiency of recombination in yeast, by using hybridization analysis, PCR, sequencing, or the like.

For homologous recombination, constructs can be prepared where the amplifiable gene will be flanked, normally on both sides with DNA homologous with the DNA of the target region. Depending upon the nature of the integrating DNA and the purpose of the integration, the homologous DNA will generally be within 100 kb, usually 50 kb, preferably about 25 kb, of the transcribed region of the target gene, more preferably within 2 kb of the target gene. Where modeling of the gene is intended, homology will usually be present proximal to the site of the mutation. The homologous DNA may include the 5′-upstream region outside of the transcriptional regulatory region or comprising any enhancer sequences, transcriptional initiation sequences, adjacent sequences, or the like. The homologous region may include a portion of the coding region, where the coding region may be comprised only of an open reading frame or combination of exons and introns. The homologous region may comprise all or a portion of an intron, where all or a portion of one or more exons may also be present. Alternatively, the homologous region may comprise the 3′-region, so as to comprise all or a portion of the transcriptional termination region, or the region 3′ of this region. The homologous regions may extend over all or a portion of the target gene or be outside the target gene comprising all or a portion of the transcriptional regulatory regions and/or the structural gene.

The integrating constructs may be prepared in accordance with conventional ways, where sequences may be synthesized, isolated from natural sources, manipulated, cloned, ligated, subjected to in vitro mutagenesis, primer repair, or the like. At various stages, the joined sequences may be cloned and analyzed by restriction analysis, sequencing, or the like. Usually during the preparation of a construct where various fragments are joined, the fragments, intermediate constructs and constructs will be carried on a cloning vector comprising a replication system functional in a prokaryotic host, e.g., E. coli and a marker for selection, e.g., biocide resistance, complementation to an auxotrophic host, etc. Other functional sequences may also be present, such as polylinkers, for ease of introduction and excision of the construct or portions thereof, or the like. A large number of cloning vectors are available such as pBR322, the pUC series, etc. These constructs may then be used for integration into the primary mammalian host.

In the case of the primary mammalian host, a replicating vector may be used. Usually, such vector will have a viral replication system, such as SV40, bovine papilloma virus, adenovirus, or the like. The linear DNA sequence vector may also have a selectable marker for identifying transfected cells. Selectable markers include the neo gene, allowing for selection with G418, the herpes tk gene for selection with HAT medium, the gpt gene with mycophenolic acid, complementation of an auxotrophic host, etc.

The vector may or may not be capable of stable maintenance in the host. Where the vector is capable of stable maintenance, the cells will be screened for homologous integration of the vector into the genome of the host, where various techniques for curing the cells may be employed. Where the vector is not capable of stable maintenance, for example, where a temperature sensitive replication system is employed, one may change the temperature from the permissive temperature to the non-permissive temperature, so that the cells may be cured of the vector. In this case, only those cells having integration of the construct comprising the amplifiable gene and, when present, the selectable marker, will be able to survive selection.

Where a selectable marker is present, one may select for the presence of the targeting construct by means of the selectable marker. Where the selectable marker is not present, one may select for the presence of the construct by the amplifiable gene. For the neo gene or the herpes tk gene, one could employ a medium for growth of the transformants of about 0.1-1 mg/ml of G418 or may use HAT medium, respectively. Where DHFR is the amplifiable gene, the selective medium may include from about 0.01-0.5 M of methotrexate or be deficient in glycine-hypoxanthine-thymidine and have dialysed serum (GHT media).

The DNA can be introduced into the expression host by a variety of techniques that include calcium phosphate/DNA co-precipitates, microinjection of DNA into the nucleus, electroporation, yeast protoplast fusion with intact cells, transfection, polycations, e.g., polybrene, polyornithine, etc., or the like. The DNA may be single or double stranded DNA, linear or circular. The various techniques for transforming mammalian cells are well known (see Keown et al., Methods Enzymol. (1989); Keown et al., Methods Enzymol. 185:527-537 (1990); Mansour et al., Nature 336:348-352, (1988); all of which are herein incorporated by reference in their entirety).

(d) Insect Constructs and Transformed Insect Cells

The present invention also relates to an insect recombinant vectors comprising exogenous genetic material. The present invention also relates to an insect cell comprising an insect recombinant vector. The present invention also relates to methods for obtaining a recombinant insect host cell, comprising introducing into an insect cell exogenous genetic material. In a preferred embodiment the exogenous genetic material includes a nucleic acid molecule of the present invention having a sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341 or complements thereof or fragments of either or other nucleic acid molecule of the present invention.

The insect recombinant vector may be any vector which can be conveniently subjected to recombinant DNA procedures and can bring about the expression of the nucleic acid sequence. The choice of a vector will typically depend on the compatibility of the vector with the insect host cell into which the vector is to be introduced. The vector may be a linear or a closed circular plasmid. The vector system may be a single vector or plasmid or two or more vectors or plasmids which together contain the total DNA to be introduced into the genome of the insect host. In addition, the insect vector may be an expression vector. Nucleic acid molecules can be suitably inserted into a replication vector for expression in the insect cell under a suitable promoter for insect cells. Many vectors are available for this purpose and selection of the appropriate vector will depend mainly on the size of the nucleic acid molecule to be inserted into the vector and the particular host cell to be transformed with the vector. Each vector contains various components depending on its function (amplification of DNA or expression of DNA) and the particular host cell with which it is compatible. The vector components for insect cell transformation generally include, but are not limited to, one or more of the following: a signal sequence, origin of replication, one or more marker genes and an inducible promoter.

The insect vector may be an autonomously replicating vector, i.e., a vector which exists as an extrachromosomal entity, the replication of which is independent of chromosomal replication, e.g., a plasmid, an extrachromosomal element, a minichromosome, or an artificial chromosome. The vector may contain any means for assuring self-replication. Alternatively, the vector may be one which, when introduced into the insect cell, is integrated into the genome and replicated together with the chromosome(s) into which it has been integrated. For integration, the vector may rely on the nucleic acid sequence of the vector for stable integration of the vector into the genome by homologous or nonhomologous recombination. Alternatively, the vector may contain additional nucleic acid sequences for directing integration by homologous recombination into the genome of the insect host. The additional nucleic acid sequences enable the vector to be integrated into the host cell genome at a precise location(s) in the chromosome(s). To increase the likelihood of integration at a precise location, there should be preferably two nucleic acid sequences which individually contain a sufficient number of nucleic acids, preferably 400 bp to 1500 bp, more preferably 800 bp to 1000 bp, which are highly homologous with the corresponding target sequence to enhance the probability of homologous recombination. These nucleic acid sequences may be any sequence that is homologous with a target sequence in the genome of the insect host cell and, furthermore, may be non-encoding or encoding sequences.

Baculovirus expression vectors (BEVs) have become important tools for the expression of foreign genes, both for basic research and for the production of proteins with direct clinical applications in human and veterinary medicine (Doerfler, Curr. Top. Microbiol. Immunol. 131:51-68 (1968); Luckow and Summers, Bio/Technology 6:47-55 (1988a); Miller, Annual Review of Microbiol. 42:177-199 (1988); Summers, Curr. Comm. Molecular Biology, Cold Spring Harbor Press, Cold Spring Harbor, N.Y. (1988); all of which are herein incorporated by reference in their entirety). BEVs are recombinant insect viruses in which the coding sequence for a chosen foreign gene has been inserted behind a baculovirus promoter in place of the viral gene, e.g., polyhedrin (Smith and Summers, U.S. Pat. No. 4,745,051, the entirety of which is incorporated herein by reference).

The use of baculovirus vectors relies upon the host cells being derived from Lepidopteran insects such as Spodoptera frugiperda or Trichoplusia ni. The preferred Spodoptera frugiperda cell line is the cell line Sf9. The Spodoptera frugiperda Sf9 cell line was obtained from American Type Culture Collection (Manassas, Va.) and is assigned accession number ATCC CRL 1711 (Summers and Smith, A Manual of Methods for Baculovirus Vectors and Insect Cell Culture Procedures, Texas Ag. Exper. Station Bulletin No. 1555 (1988), the entirety of which is herein incorporated by reference). Other insect cell systems, such as the silkworm B. mori may also be used.

The proteins expressed by the BEVs are, therefore, synthesized, modified and transported in host cells derived from Lepidopteran insects. Most of the genes that have been inserted and produced in the baculovirus expression vector system have been derived from vertebrate species. Other baculovirus genes in addition to the polyhedrin promoter may be employed to advantage in a baculovirus expression system. These include immediate-early (alpha), delayed-early ( ), late ( ), or very late (delta), according to the phase of the viral infection during which they are expressed. The expression of these genes occurs sequentially, probably as the result of a “cascade” mechanism of transcriptional regulation. (Guarino and Summers, J. Virol. 57:563-571 (1986); Guarino and Summers, J. Virol. 61:2091-2099 (1987); Guarino and Summers, Virol. 162:444-451 (1988); all of which are herein incorporated by reference in their entirety).

Insect recombinant vectors are useful as intermediates for the infection or transformation of insect cell systems. For example, an insect recombinant vector containing a nucleic acid molecule encoding a baculovirus transcriptional promoter followed downstream by an insect signal DNA sequence is capable of directing the secretion of the desired biologically active protein from the insect cell. The vector may utilize a baculovirus transcriptional promoter region derived from any of the over 500 baculoviruses generally infecting insects, such as for example the Orders Lepidoptera, Diptera, Orthoptera, Coleoptera and Hymenoptera, including for example but not limited to the viral DNAs of Autographa californica MNPV, Bombyx mori NPV, Trichoplusia ni MNPV, Rachiplusia ou MNPV or Galleria mellonella MNPV, wherein said baculovirus transcriptional promoter is a baculovirus immediate-early gene IEl or IEN promoter; an immediate-early gene in combination with a baculovirus delayed-early gene promoter region selected from the group consisting of 39K and a HindIII-k fragment delayed-early gene; or a baculovirus late gene promoter. The immediate-early or delayed-early promoters can be enhanced with transcriptional enhancer elements. The insect signal DNA sequence may code for a signal peptide of a Lepidopteran adipokinetic hormone precursor or a signal peptide of the Manduca sexta adipokinetic hormone precursor (Summers, U.S. Pat. No. 5,155,037; the entirety of which is herein incorporated by reference). Other insect signal DNA sequences include a signal peptide of the Orthoptera Schistocerca gregaria locust adipokinetic hormone precursor and the Drosophila melanogaster cuticle genes CP1, CP2, CP3 or CP4 or for an insect signal peptide having substantially a similar chemical composition and function (Summers, U.S. Pat. No. 5,155,037).

Insect cells are distinctly different from animal cells. Insects have a unique life cycle and have distinct cellular properties such as the lack of intracellular plasminogen activators in which are present in vertebrate cells. Another difference is the high expression levels of protein products ranging from 1 to greater than 500 mg/liter and the ease at which cDNA can be cloned into cells (Frasier, In Vitro Cell. Dev. Biol. 25:225 (1989); Summers and Smith, In: A Manual of Methods for Baculovirus Vectors and Insect Cell Culture Procedures, Texas Ag. Exper. Station Bulletin No. 1555 (1988), both of which are incorporated by reference in their entirety).

Recombinant protein expression in insect cells is achieved by viral infection or stable transformation. For viral infection, the desired gene is cloned into baculovirus at the site of the wild-type polyhedron gene (Webb and Summers, Technique 2:173 (1990); Bishop and Posse, Adv. Gene Technol. 1:55 (1990); both of which are incorporated by reference in their entirety). The polyhedron gene is a component of a protein coat in occlusions which encapsulate virus particles. Deletion or insertion in the polyhedron gene results the failure to form occlusion bodies. Occlusion negative viruses are morphologically different from occlusion positive viruses and enable one skilled in the art to identify and purify recombinant viruses.

The vectors of present invention preferably contain one or more selectable markers which permit easy selection of transformed cells. A selectable marker is a gene the product of which provides, for example biocide or viral resistance, resistance to heavy metals, prototrophy to auxotrophs and the like. Selection may be accomplished by co-transformation, e.g., as described in WO 91/17243, a nucleic acid sequence of the present invention may be operably linked to a suitable promoter sequence. The promoter sequence is a nucleic acid sequence which is recognized by the insect host cell for expression of the nucleic acid sequence. The promoter sequence contains transcription and translation control sequences which mediate the expression of the protein or fragment thereof. The promoter may be any nucleic acid sequence which shows transcriptional activity in the insect host cell of choice and may be obtained from genes encoding polypeptides either homologous or heterologous to the host cell.

For example, a nucleic acid molecule encoding a protein or fragment thereof may also be operably linked to a suitable leader sequence. A leader sequence is a nontranslated region of a mRNA which is important for translation by the fungal host. The leader sequence is operably linked to the 5′ terminus of the nucleic acid sequence encoding the protein or fragment thereof. The leader sequence may be native to the nucleic acid sequence encoding the protein or fragment thereof or may be obtained from foreign sources. Any leader sequence which is functional in the insect host cell of choice may be used in the present invention.

A polyadenylation sequence may also be operably linked to the 3′ terminus of the nucleic acid sequence of the present invention. The polyadenylation sequence is a sequence which when transcribed is recognized by the insect host to add polyadenosine residues to transcribed mRNA. The polyadenylation sequence may be native to the nucleic acid sequence encoding the protein or fragment thereof or may be obtained from foreign sources. Any polyadenylation sequence which is functional in the fungal host of choice may be used in the present invention.

To avoid the necessity of disrupting the cell to obtain the protein or fragment thereof and to minimize the amount of possible degradation of the expressed polypeptide within the cell, it is preferred that expression of the polypeptide gene gives rise to a product secreted outside the cell. To this end, the protein or fragment thereof of the present invention may be linked to a signal peptide linked to the amino terminus of the protein or fragment thereof. A signal peptide is an amino acid sequence which permits the secretion of the protein or fragment thereof from the insect host into the culture medium. The signal peptide may be native to the protein or fragment thereof of the invention or may be obtained from foreign sources. The 5′ end of the coding sequence of the nucleic acid sequence of the present invention may inherently contain a signal peptide coding region naturally linked in translation reading frame with the segment of the coding region which encodes the secreted protein or fragment thereof.

At present, a mode of achieving secretion of a foreign gene product in insect cells is by way of the foreign gene's native signal peptide. Because the foreign genes are usually from non-insect organisms, their signal sequences may be poorly recognized by insect cells and hence, levels of expression may be suboptimal. However, the efficiency of expression of foreign gene products seems to depend primarily on the characteristics of the foreign protein. On average, nuclear localized or non-structural proteins are most highly expressed, secreted proteins are intermediate and integral membrane proteins are the least expressed. One factor generally affecting the efficiency of the production of foreign gene products in a heterologous host system is the presence of native signal sequences (also termed presequences, targeting signals, or leader sequences) associated with the foreign gene. The signal sequence is generally coded by a DNA sequence immediately following (5′ to 3′) the translation start site of the desired foreign gene.

The expression dependence on the type of signal sequence associated with a gene product can be represented by the following example: If a foreign gene is inserted at a site downstream from the translational start site of the baculovirus polyhedrin gene so as to produce a fusion protein (containing the N-terminus of the polyhedrin structural gene), the fused gene is highly expressed. But less expression is achieved when a foreign gene is inserted in a baculovirus expression vector immediately following the transcriptional start site and totally replacing the polyhedrin structural gene.

Insertions into the region −50 to −1 significantly alter (reduce) steady state transcription which, in turn, reduces translation of the foreign gene product. Use of the pVL941 vector optimizes transcription of foreign genes to the level of the polyhedrin gene transcription. Even though the transcription of a foreign gene may be optimal, optimal translation may vary because of several factors involving processing: signal peptide recognition, mRNA and ribosome binding, glycosylation, disulfide bond formation, sugar processing, oligomerization, for example.

The properties of the insect signal peptide are expected to be more optimal for the efficiency of the translation process in insect cells than those from vertebrate proteins. This phenomenon can generally be explained by the fact that proteins secreted from cells are synthesized as precursor molecules containing hydrophobic N-terminal signal peptides. The signal peptides direct transport of the select protein to its target membrane and are then cleaved by a peptidase on the membrane, such as the endoplasmic reticulum, when the protein passes through it.

Another exemplary insect signal sequence is the sequence encoding for Drosophila cuticle proteins such as CP1, CP2, CP3 or CP4 (Summers, U.S. Pat. No. 5,278,050; the entirety of which is herein incorporated by reference). Most of a 9 kb region of the Drosophila genome containing genes for the cuticle proteins has been sequenced. Four of the five cuticle genes contains a signal peptide coding sequence interrupted by a short intervening sequence (about 60 base pairs) at a conserved site. Conserved sequences occur in the 5′ mRNA untranslated region, in the adjacent 35 base pairs of upstream flanking sequence and at −200 base pairs from the mRNA start position in each of the cuticle genes.

Standard methods of insect cell culture, cotransfection and preparation of plasmids are set forth in Summers and Smith (Summers and Smith, A Manual of Methods for Baculovirus Vectors and Insect Cell Culture Procedures, Texas Agricultural Experiment Station Bulletin No. 1555, Texas A&M University (1987)). Procedures for the cultivation of viruses and cells are described in Volkman and Summers, J. Virol 19:820-832 (1975) and Volkman et al., J. Virol 19:820-832 (1976); both of which are herein incorporated by reference in their entirety.

(e) Bacterial Constructs and Transformed Bacterial Cells

The present invention also relates to a bacterial recombinant vector comprising exogenous genetic material. The present invention also relates to a bacteria cell comprising a bacterial recombinant vector. The present invention also relates to methods for obtaining a recombinant bacteria host cell, comprising introducing into a bacterial host cell exogenous genetic material. In a preferred embodiment the exogenous genetic material includes a nucleic acid molecule of the present invention having a sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341 or complements thereof or fragments of either or other nucleic acid molecule of the present invention.

The bacterial recombinant vector may be any vector which can be conveniently subjected to recombinant DNA procedures. The choice of a vector will typically depend on the compatibility of the vector with the bacterial host cell into which the vector is to be introduced. The vector may be a linear or a closed circular plasmid. The vector system may be a single vector or plasmid or two or more vectors or plasmids which together contain the total DNA to be introduced into the genome of the bacterial host. In addition, the bacterial vector may be an expression vector. Nucleic acid molecules encoding protein homologues or fragments thereof can, for example, be suitably inserted into a replicable vector for expression in the bacterium under the control of a suitable promoter for bacteria. Many vectors are available for this purpose and selection of the appropriate vector will depend mainly on the size of the nucleic acid to be inserted into the vector and the particular host cell to be transformed with the vector. Each vector contains various components depending on its function (amplification of DNA or expression of DNA) and the particular host cell with which it is compatible. The vector components for bacterial transformation generally include, but are not limited to, one or more of the following: a signal sequence, an origin of replication, one or more marker genes and an inducible promoter.

In general, plasmid vectors containing replicon and control sequences that are derived from species compatible with the host cell are used in connection with bacterial hosts. The vector ordinarily carries a replication site, as well as marking sequences that are capable of providing phenotypic selection in transformed cells. For example, E. coli is typically transformed using pBR322, a plasmid derived from an E. coli species (see, e.g., Bolivar et al., Gene 2:95 (1977); the entirety of which is herein incorporated by reference). pBR322 contains genes for ampicillin and tetracycline resistance and thus provides easy means for identifying transformed cells. The pBR322 plasmid, or other microbial plasmid or phage, also generally contains, or is modified to contain, promoters that can be used by the microbial organism for expression of the selectable marker genes.

Nucleic acid molecules encoding protein or fragments thereof may be expressed not only directly, but also as a fusion with another polypeptide, preferably a signal sequence or other polypeptide having a specific cleavage site at the N-terminus of the mature polypeptide. In general, the signal sequence may be a component of the vector, or it may be a part of the polypeptide DNA that is inserted into the vector. The heterologous signal sequence selected should be one that is recognized and processed (i.e., cleaved by a signal peptidase) by the host cell. For bacterial host cells that do not recognize and process the native polypeptide signal sequence, the signal sequence is substituted by a bacterial signal sequence selected, for example, from the group consisting of the alkaline phosphatase, penicillinase, lpp, or heat-stable enterotoxin II leaders.

Both expression and cloning vectors contain a nucleic acid sequence that enables the vector to replicate in one or more selected host cells. Generally, in cloning vectors this sequence is one that enables the vector to replicate independently of the host chromosomal DNA and includes origins of replication or autonomously replicating sequences. Such sequences are well known for a variety of bacteria. The origin of replication from the plasmid pBR322 is suitable for most Gram-negative bacteria.

Expression and cloning vectors also generally contain a selection gene, also termed a selectable marker. This gene encodes a protein necessary for the survival or growth of transformed host cells grown in a selective culture medium. Host cells not transformed with the vector containing the selection gene will not survive in the culture medium. Typical selection genes encode proteins that (a) confer resistance to antibiotics or other toxins, e.g., ampicillin, neomycin, methotrexate, or tetracycline, (b) complement auxotrophic deficiencies, or (c) supply critical nutrients not available from complex media, e.g., the gene encoding D-alanine racemase for Bacilli. One example of a selection scheme utilizes a drug to arrest growth of a host cell. Those cells that are successfully transformed with a heterologous protein homologue or fragment thereof produce a protein conferring drug resistance and thus survive the selection regimen.

The expression vector for producing a protein or fragment thereof can also contains an inducible promoter that is recognized by the host bacterial organism and is operably linked to the nucleic acid encoding, for example, the nucleic acid molecule encoding the protein homologue or fragment thereof of interest. Inducible promoters suitable for use with bacterial hosts include the -lactamase and lactose promoter systems (Chang et al., Nature 275:615 (1978); Goeddel et al., Nature 281:544 (1979); both of which are herein incorporated by reference in their entirety), the arabinose promoter system (Guzman et al., J. Bacteriol. 174:7716-7728 (1992); the entirety of which is herein incorporated by reference), alkaline phosphatase, a tryptophan (trp) promoter system (Goeddel, Nucleic Acids Res. 8:4057 (1980); EP 36,776; both of which are herein incorporated by reference in their entirety) and hybrid promoters such as the tac promoter (deBoer et al., Proc. Natl. Acad. Sci. (USA) 80:21-25 (1983); the entirety of which is herein incorporated by reference). However, other known bacterial inducible promoters are suitable (Siebenlist et al., Cell 20:269 (1980); the entirety of which is herein incorporated by reference).

Promoters for use in bacterial systems also generally contain a Shine-Dalgarno (S.D.) sequence operably linked to the DNA encoding the polypeptide of interest. The promoter can be removed from the bacterial source DNA by restriction enzyme digestion and inserted into the vector containing the desired DNA.

Construction of suitable vectors containing one or more of the above-listed components employs standard ligation techniques. Isolated plasmids or DNA fragments are cleaved, tailored and re-ligated in the form desired to generate the plasmids required. Examples of available bacterial expression vectors include, but are not limited to, the multifunctional E. coli cloning and expression vectors such as Bluescript™ (Stratagene, La Jolla, Calif.), in which, for example, encoding an A. nidulans protein homologue or fragment thereof homologue, may be ligated into the vector in frame with sequences for the amino-terminal Met and the subsequent 7 residues of -galactosidase so that a hybrid protein is produced; pIN vectors (Van Heeke and Schuster, J. Biol. Chem. 264:5503-5509 (1989), the entirety of which is herein incorporated by reference); and the like. pGEX vectors (Promega, Madison Wis. U.S.A.) may also be used to express foreign polypeptides as fusion proteins with glutathione S-transferase (GST). In general, such fusion proteins are soluble and can easily be purified from lysed cells by adsorption to glutathione-agarose beads followed by elution in the presence of free glutathione. Proteins made in such systems are designed to include heparin, thrombin or factor XA protease cleavage sites so that the cloned polypeptide of interest can be released from the GST moiety at will.

Suitable host bacteria for a bacterial vector include archaebacteria and eubacteria, especially eubacteria and most preferably Enterobacteriaceae. Examples of useful bacteria include Escherichia, Enterobacter, Azotobacter, Erwinia, Bacillus, Pseudomonas, Klebsiella, Proteus, Salmonella, Serratia, Shigella, Rhizobia, Vitreoscilla and Paracoccus. Suitable E. coli hosts include E. coli W3110 (American Type Culture Collection (ATCC) 27,325, Manassas, Va. U.S.A.), E. coli 294 (ATCC 31,446), E. coli B and E. coli X1776 (ATCC 31,537). These examples are illustrative rather than limiting. Mutant cells of any of the above-mentioned bacteria may also be employed. It is, of course, necessary to select the appropriate bacteria taking into consideration replicability of the replicon in the cells of a bacterium. For example, E. coli, Serratia, or Salmonella species can be suitably used as the host when well known plasmids such as pBR322, pBR325, pACYC177, or pKN410 are used to supply the replicon. E. coli strain W3110 is a preferred host or parent host because it is a common host strain for recombinant DNA product fermentations. Preferably, the host cell should secrete minimal amounts of proteolytic enzymes.

Host cells are transfected and preferably transformed with the above-described vectors and cultured in conventional nutrient media modified as appropriate for inducing promoters, selecting transformants, or amplifying the genes encoding the desired sequences.

Numerous methods of transfection are known to the ordinarily skilled artisan, for example, calcium phosphate and electroporation. Depending on the host cell used, transformation is done using standard techniques appropriate to such cells. The calcium treatment employing calcium chloride, as described in section 1.82 of Sambrook et al., Molecular Cloning: A Laboratory Manual, New York: Cold Spring Harbor Laboratory Press, (1989), is generally used for bacterial cells that contain substantial cell-wall barriers. Another method for transformation employs polyethylene glycol/DMSO, as described in Chung and Miller (Chung and Miller, Nucleic Acids Res. 16:3580 (1988); the entirety of which is herein incorporated by reference). Yet another method is the use of the technique termed electroporation.

Bacterial cells used to produce the polypeptide of interest for purposes of this invention are cultured in suitable media in which the promoters for the nucleic acid encoding the heterologous polypeptide can be artificially induced as described generally, e.g., in Sambrook et al., Molecular Cloning: A Laboratory Manual, New York: Cold Spring Harbor Laboratory Press, (1989). Examples of suitable media are given in U.S. Pat. Nos. 5,304,472 and 5,342,763; both of which are incorporated by reference in their entirety.

In addition to the above discussed procedures, practitioners are familiar with the standard resource materials which describe specific conditions and procedures for the construction, manipulation and isolation of macromolecules (e.g., DNA molecules, plasmids, etc.), generation of recombinant organisms and the screening and isolating of clones, (see for example, Sambrook et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Press (1989); Mailga et al., Methods in Plant Molecular Biology, Cold Spring Harbor Press (1995), the entirety of which is herein incorporated by reference; Birren et al., Genome Analysis: Analyzing DNA, 1, Cold Spring Harbor, N.Y., the entirety of which is herein incorporated by reference).

(f) Computer Readable Media

The nucleotide sequence provided in SEQ ID NO: 1 through SEQ ID NO: 7341 or fragment thereof, or complement thereof, or a nucleotide sequence at least 90% identical, preferably 95%, identical even more preferably 99% or 100% identical to the sequence provided in SEQ ID NO: 1 through SEQ ID NO: 7341 or fragment thereof, or complement thereof, can be “provided” in a variety of mediums to facilitate use. Such a medium can also provide a subset thereof in a form that allows a skilled artisan to examine the sequences.

A preferred subset of nucleotide sequences are those nucleic acid sequences that encode a maize or soybean ribulose-bisphosphate carboxylase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean phosphoglycerate kinase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean glyceraldehyde 3-phosphate dehydrogenase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a putative maize glyceraldehyde 3-phosphate dehydrogenase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean triose phosphate isomerase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean aldolase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean fructose-1,6-bisphosphatase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean transketolase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a putative maize or soybean transketolase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encode a maize or soybean sedoheptulose-1,7-bisphosphatase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean D-ribulose-5-phosphate-3-epimerase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean ribose-5-phosphate isomerase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a putative maize or soybean ribose-5-phosphate isomerase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean ribose-5-phosphate kinase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean phosphoenolpyruvate carboxylase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean NADP-dependent malate dehydrogenase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean aspartate aminotransferase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a putative maize or soybean aspartate aminotransferase enzyme or complement thereof or fragment of either, nucleic acid sequences that encode a maize or soybean alanine aminotransferase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean NADP-dependent malic enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean NAD-dependent malic enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean PEP carboxykinase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a putative soybean PEP carboxykinase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean pyruvate, phosphate dikinase enzyme or complement thereof or fragment of either and a nucleic acid molecule that encodes a maize or soybean pyrophosphatase enzyme or complement thereof or fragment of either.

A further preferred subset of nucleic acid sequences is where the subset of sequences which encode two proteins or fragments thereof, more preferably three proteins or fragments thereof, more preferable four proteins or fragments thereof, more preferably five proteins or fragments thereof, more preferable six proteins or fragments thereof, more preferably seven proteins or fragments thereof, more preferably eight proteins or fragments thereof, more preferable nine proteins or fragments thereof, more preferably ten proteins or fragments thereof, more preferably eleven proteins or fragments thereof, more preferable twelve proteins or fragments thereof, more preferably thirteen proteins or fragments thereof, more preferably fourteen proteins or fragments thereof, more preferable fifteen proteins or fragments thereof, more preferably sixteen proteins or fragments thereof, more preferably seventeen proteins or fragments thereof, more preferable eighteen proteins or fragments thereof, more preferably nineteen proteins or fragments thereof, more preferably twenty proteins or fragments thereof more preferably twenty one proteins or fragments thereof, more preferable twenty two proteins or fragments thereof, more preferably twenty three proteins or fragments thereof, more preferably twenty four proteins or fragments thereof, and even more preferably twenty five proteins or fragments thereof. These nucleic acid sequences are selected from the group that encodes a maize or soybean ribulose-bisphosphate carboxylase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean phosphoglycerate kinase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean glyceraldehyde 3-phosphate dehydrogenase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a putative maize glyceraldehyde 3-phosphate dehydrogenase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean triose phosphate isomerase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean aldolase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean fructose-1,6-bisphosphatase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean transketolase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a putative maize or soybean transketolase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encode a maize or soybean sedoheptulose-1,7-bisphosphatase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean D-ribulose-5-phosphate-3-epimerase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean ribose-5-phosphate isomerase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a putative maize or soybean ribose-5-phosphate isomerase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean ribose-5-phosphate kinase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean phosphoenolpyruvate carboxylase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean NADP-dependent malate dehydrogenase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean aspartate aminotransferase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a putative maize or soybean aspartate aminotransferase enzyme or complement thereof or fragment of either, nucleic acid sequences that encode a maize or soybean alanine aminotransferase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean NADP-dependent malic enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean NAD-dependent malic enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a maize or soybean PEP carboxykinase enzyme or complement thereof or fragment of either, a nucleic acid molecule that encodes a putative soybean PEP carboxykinase enzyme or complement thereof or fragment either, a nucleic acid molecule that encodes a maize or soybean pyruvate, phosphate dikinase enzyme or complement thereof or fragment of either and a nucleic acid molecule that encodes a maize or soybean pyrophosphatase enzyme or complement thereof or fragment of either.

In one application of this embodiment, a nucleotide sequence of the present invention can be recorded on computer readable media. As used herein, “computer readable media” refers to any medium that can be read and accessed directly by a computer. Such media include, but are not limited to: magnetic storage media, such as floppy discs, hard disc, storage medium and magnetic tape: optical storage media such as CD-ROM; electrical storage media such as RAM and ROM; and hybrids of these categories such as magnetic/optical storage media. A skilled artisan can readily appreciate how any of the presently known computer readable mediums can be used to create a manufacture comprising computer readable medium having recorded thereon a nucleotide sequence of the present invention.

As used herein, “recorded” refers to a process for storing information on computer readable medium. A skilled artisan can readily adopt any of the presently known methods for recording information on computer readable medium to generate media comprising the nucleotide sequence information of the present invention. A variety of data storage structures are available to a skilled artisan for creating a computer readable medium having recorded thereon a nucleotide sequence of the present invention. The choice of the data storage structure will generally be based on the means chosen to access the stored information. In addition, a variety of data processor programs and formats can be used to store the nucleotide sequence information of the present invention on computer readable medium. The sequence information can be represented in a word processing text file, formatted in commercially-available software such as WordPerfect and Microsoft Word, or represented in the form of an ASCII file, stored in a database application, such as DB2, Sybase, Oracle, or the like. A skilled artisan can readily adapt any number of data processor structuring formats (e.g. text file or database) in order to obtain computer readable medium having recorded thereon the nucleotide sequence information of the present invention.

By providing one or more of nucleotide sequences of the present invention, a skilled artisan can routinely access the sequence information for a variety of purposes. Computer software is publicly available which allows a skilled artisan to access sequence information provided in a computer readable medium. The examples which follow demonstrate how software which implements the BLAST (Altschul et al., J. Mol. Biol. 215:403-410 (1990), the entirety of which is herein incorporated by reference) and BLAZE (Brutlag et al., Comp. Chem. 17:203-207 (1993), the entirety of which is herein incorporated by reference) search algorithms on a Sybase system can be used to identify open reading frames (ORFs) within the genome that contain homology to ORFs or proteins from other organisms. Such ORFs are protein-encoding fragments within the sequences of the present invention and are useful in producing commercially important proteins such as enzymes used in amino acid biosynthesis, metabolism, transcription, translation, RNA processing, nucleic acid and a protein degradation, protein modification and DNA replication, restriction, modification, recombination and repair.

The present invention further provides systems, particularly computer-based systems, which contain the sequence information described herein. Such systems are designed to identify commercially important fragments of the nucleic acid molecule of the present invention. As used herein, “a computer-based system” refers to the hardware means, software means and data storage means used to analyze the nucleotide sequence information of the present invention. The minimum hardware means of the computer-based systems of the present invention comprises a central processing unit (CPU), input means, output means and data storage means. A skilled artisan can readily appreciate that any one of the currently available computer-based system are suitable for use in the present invention.

As indicated above, the computer-based systems of the present invention comprise a data storage means having stored therein a nucleotide sequence of the present invention and the necessary hardware means and software means for supporting and implementing a search means. As used herein, “data storage means” refers to memory that can store nucleotide sequence information of the present invention, or a memory access means which can access manufactures having recorded thereon the nucleotide sequence information of the present invention. As used herein, “search means” refers to one or more programs which are implemented on the computer-based system to compare a target sequence or target structural motif with the sequence information stored within the data storage means. Search means are used to identify fragments or regions of the sequence of the present invention that match a particular target sequence or target motif. A variety of known algorithms are disclosed publicly and a variety of commercially available software for conducting search means are available can be used in the computer-based systems of the present invention. Examples of such software include, but are not limited to, MacPattern (EMBL), BLASTIN and BLASTIX (NCBIA). One of the available algorithms or implementing software packages for conducting homology searches can be adapted for use in the present computer-based systems.

The most preferred sequence length of a target sequence is from about 10 to 100 amino acids or from about 30 to 300 nucleotide residues. However, it is well recognized that during searches for commercially important fragments of the nucleic acid molecules of the present invention, such as sequence fragments involved in gene expression and protein processing, may be of shorter length.

As used herein, “a target structural motif,” or “target motif,” refers to any rationally selected sequence or combination of sequences in which the sequences the sequence(s) are chosen based on a three-dimensional configuration which is formed upon the folding of the target motif. There are a variety of target motifs known in the art. Protein target motifs include, but are not limited to, enzymatic active sites and signal sequences. Nucleic acid target motifs include, but are not limited to, promoter sequences, cis elements, hairpin structures and inducible expression elements (protein binding sequences).

Thus, the present invention further provides an input means for receiving a target sequence, a data storage means for storing the target sequences of the present invention sequence identified using a search means as described above and an output means for outputting the identified homologous sequences. A variety of structural formats for the input and output means can be used to input and output information in the computer-based systems of the present invention. A preferred format for an output means ranks fragments of the sequence of the present invention by varying degrees of homology to the target sequence or target motif. Such presentation provides a skilled artisan with a ranking of sequences which contain various amounts of the target sequence or target motif and identifies the degree of homology contained in the identified fragment.

A variety of comparing means can be used to compare a target sequence or target motif with the data storage means to identify sequence fragments sequence of the present invention. For example, implementing software which implement the BLAST and BLAZE algorithms (Altschul et al., J. Mol. Biol. 215:403-410 (1990)) can be used to identify open frames within the nucleic acid molecules of the present invention. A skilled artisan can readily recognize that any one of the publicly available homology search programs can be used as the search means for the computer-based systems of the present invention.

Having now generally described the invention, the same will be more readily understood through reference to the following examples which are provided by way of illustration and are not intended to be limiting of the present invention, unless specified.

EXAMPLE 1

The MONN01 cDNA library is a normalized library generated from maize (DK604, Dekalb Genetics, Dekalb, Ill. U.S.A.) total leaf tissue at the V6 plant development stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the greenhouse in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Tissue is collected when the maize plant is at the 6-leaf development stage. The older, more juvenile leaves, which are in a basal position, as well as the younger, more adult leaves, which are more apical are cut at the base of the leaves. The leaves are then pooled and immediately transferred to liquid nitrogen containers in which the pooled leaves are crushed. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON001 cDNA library is generated from maize (B73, Illinois Foundation Seeds, Champaign, Ill. U.S.A.) immature tassels at the V6 plant development stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in a greenhouse in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Tissue from the maize plant is collected at the V6 stage. At that stage the tassel is an immature tassel of about 2-3 cm in length. The tassels are removed and frozen in liquid nitrogen. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON003 library is generated from maize (B73x Mo17, Illinois Foundation Seeds, Champaign, Ill. U.S.A.) roots at the V6 developmental stage. Seeds are planted at a depth of approximately 3 cm in coil into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth, the seedlings are transplanted into 10 inch pots containing the Metro 200 growing medium. Plants are watered daily before transplantation and approximately 3 times a week after transplantation. Peters 15-16-17 fertilizer is applied approximately three times per week after transplanting at a concentration of 150 ppm N. Two to three times during the life time of the plant from transplanting to flowering a total of approximately 900 mg Fe is added to each pot. Maize plants are grown in the green house in approximately 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Tissue is collected when the maize plant is at the 6 leaf development stage. The root system is cut from maize plant and washed with water to free it from the soil. The tissue is then immediately frozen in liquid nitrogen. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON004 cDNA library is generated from maize (B73x Mo17, Illinois Foundation Seeds, Champaign, Ill. U.S.A.) total leaf tissue at the V6 plant development stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the greenhouse in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Tissue is collected when the maize plant is at the 6-leaf development stage. The older, more juvenile leaves, which are in a basal position, as well as the younger, more adult leaves, which are more apical are cut at the base of the leaves. The leaves are then pooled and immediately transferred to liquid nitrogen containers in which the pooled leaves are crushed. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON005 cDNA library is generated from maize (B73x Mo17, Illinois Foundation Seeds, Champaign Ill., U.S.A.) root tissue at the V6 development stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the green house in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Tissue is collected when the maize plant is at the 6-leaf development stage. The root system is cut from the mature maize plant and washed with water to free it from the soil. The tissue is immediately frozen in liquid nitrogen and the harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON006 cDNA library is generated from maize (B73x Mo17, Illinois Foundation Seeds, Champaign Ill., U.S.A.) total leaf tissue at the V6 plant development stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the greenhouse in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Tissue is collected when the maize plant is at the 6-leaf development stage. The older more juvenile leaves, which are in a basal position, as well as the younger more adult leaves, which are more apical are cut at the base of the leaves. The leaves are then pooled and immediately transferred to liquid nitrogen containers in which the pooled leaves are crushed. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON007 cDNA library is generated from the primary root tissue of 5 day old maize (DK604, Dekalb Genetics, Dekalb, Ill. U.S.A.) seedlings. Seeds are planted on a moist filter paper on a covered tray that is kept in the dark until germination (one day). After germination, the trays, along with the moist paper, are moved to a greenhouse where the maize plants are grown in the greenhouse in 15 hr day/9 hr night cycles for approximately 5 days. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. The primary root tissue is collected when the seedlings are 5 days old. At this stage, the primary root (radicle) is pushed through the coleorhiza which itself is pushed through the seed coat. The primary root, which is about 2-3 cm long, is cut and immediately frozen in liquid nitrogen and then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON008 cDNA library is generated from the primary shoot (coleoptile 2-3 cm) of maize (DK604, Dekalb Genetics, Dekalb, Ill. U.S.A.) seedlings which are approximately 5 days old. Seeds are planted on a moist filter paper on a covered tray that is kept in the dark until germination (one day). Then the trays containing the seeds are moved to a greenhouse at 15 hr daytime/9 hr nighttime cycles and grown until they are 5 days post germination. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Tissue is collected when the seedlings are 5 days old. At this stage, the primary shoot (coleoptile) is pushed through the seed coat and is about 2-3 cm long. The coleoptile is dissected away from the rest of the seedling, immediately frozen in liquid nitrogen and then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON009 cDNA library is generated from maize (DK604, Dekalb Genetics, Dekalb, Ill. U.S.A.) leaves at the 8 leaf stage (V8 plant development stage). Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the green house in 15 hr day/9 hr night cycles. The daytime temperature is 80° F. and the nighttime temperature is 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Tissue is collected when the maize plant is at the 8-leaf development stage. The older more juvenile leaves, which are in a basal position, as well as the younger more adult leaves, which are more apical, are cut at the base of the leaves. The leaves are then pooled and then immediately transferred to liquid nitrogen containers in which the pooled leaves are crushed. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON010 cDNA library is generated from maize (DK604, Dekalb Genetics, Dekalb, Ill. U.S.A.) root tissue at the V8 plant development stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the green house in 15 hr day/9 hr night cycles. The daytime temperature is 80° F. and the nighttime temperature is 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Tissue is collected when the maize plant is at the V8 development stage. The root system is cut from this mature maize plant and washed with water to free it from the soil. The tissue is immediately frozen in liquid nitrogen. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON011 cDNA library is generated from undeveloped maize (DK604, Dekalb Genetics, Dekalb, Ill. U.S.A.) leaf at the V6 plant development stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the green house in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Tissue is collected when the maize plant is at the 6-leaf development stage. The second youngest leaf which is at the base of the apical leaf of V6 stage maize plant is cut at the base and immediately transferred to liquid nitrogen containers in which the leaf is crushed. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON012 cDNA library is generated from 2 day post germination maize (DK604, Dekalb Genetics, Dekalb, Ill. U.S.A.) seedlings. Seeds are planted on a moist filter paper on a covered tray that is kept in the dark until germination (one day). Then the trays containing the seeds are moved to the greenhouse and grown at 15 hr daytime/9 hr nighttime cycles until 2 days post germination. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Tissue is collected when the seedlings are 2 days old. At the two day stage, the coleorhiza is pushed through the seed coat and the primary root (the radicle) is pierced the coleorhiza but is barely visible. Also, at this two day stage, the coleoptile is just emerging from the seed coat. The 2 days post germination seedlings are then immersed in liquid nitrogen and crushed. The harvested tissue is stored at −80° C. until preparation of total RNA. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON013 cDNA library is generated from apical maize (DK604, Dekalb Genetics, Dekalb, Ill. U.S.A.) meristem founder at the V4 plant development stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the greenhouse in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Prior to tissue collection, the plant is at the 4 leaf stage. The lead at the apex of the V4 stage maize plant is referred to as the meristem founder. This apical meristem founder is cut, immediately frozen in liquid nitrogen and crushed. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON014 cDNA library is generated from maize (DK604, Dekalb Genetics, Dekalb, Ill. U.S.A.) endosperm fourteen days after pollination. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the greenhouse in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. After the V10 stage, the maize plant ear shoots are ready for fertilization. At this stage, the ear shoots are enclosed in a paper bag before silk emergence to withhold the pollen. The ear shoots are pollinated and 14 days after pollination, the ears are pulled out and then the kernels are plucked out of the ears. Each kernel is then dissected into the embryo and the endosperm and the aleurone layer is removed. After dissection, the endosperms are immediately frozen in liquid nitrogen and then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON016 library is a maize (DK604, Dekalb Genetics, Dekalb, Ill. U.S.A.) sheath library collected at the V8 developmental stage. Seeds are planted in a depth of approximately 3 cm in solid into 2-3 inch pots containing Metro growing medium. After 2-3 weeks growth, they are transplanted into 10″ pots containing the same. Plants are watered daily before transplantation and approximately the times a week after transplantation. Peters 15-16-17 fertilizer is applied approximately three times per week after transplanting, at a strength of 150 ppm N. Two to three times during the life time of the plant from transplanting to flowering, a total of approximately 900 mg Fe is added to each pot. Maize plants are grown in the green house in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. When the maize plants are at the V8 stage the 5^(th) and 6^(th) leaves from the bottom exhibit fully developed leaf blades. At the base of these leaves, the ligule is differentiated and the leaf blade is joined to the sheath. The sheath is dissected away from the base of the leaf then the sheath is frozen in liquid nitrogen and crushed. The tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON017 cDNA library is generated from maize (DK604, Dekalb Genetics, Dekalb, Ill. U.S.A.) embryo seventeen days after pollination. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth the seeds are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the green house in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. After the V 10 stage, the ear shoots of maize plant, which are ready for fertilization, are enclosed in a paper bag before silk emergence to withhold the pollen. The ear shoots are fertilized and 21 days after pollination, the ears are pulled out and the kernels are plucked out of the ears. Each kernel is then dissected into the embryo and the endosperm and the aleurone layer is removed. After dissection, the embryos are immediately frozen in liquid nitrogen and then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON019 (Lib3054) cDNA library is generated from maize (DK604, Dekalb Genetics, Dekalb, Ill. U.S.A.) culm (stem) at the V8 developmental stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the green house in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. When the maize plant is at the V8 stage, the 5th and 6th leaves from the bottom have fully developed leaf blades. The region between the nodes of the 5th and the sixth leaves from the bottom is the region of the stem that is collected. The leaves are pulled out and the sheath is also torn away from the stem. This stem tissue is completely free of any leaf and sheath tissue. The stem tissue is then frozen in liquid nitrogen and stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON020 cDNA library is from a maize (DK604, Dekalb Genetics, Dekalb, Ill. U.S.A.) Hill Type II-Initiated Callus. Petri plates containing approximately 25 ml of Type II initiation media are prepared. This medium contains N6 salts and vitamins, 3% sucrose, 2.3 g/liter proline 0.1 g/liter enzymatic casein hydrolysate, 2 mg/liter 2,4-dichloro phenoxy-acetic acid (2,4, D), 15.3 mg/liter AgNO₃ and 0.8% bacto agar and is adjusted to pH 6.0 before autoclaving. At 9-11 days after pollination, an ear with immature embryos measuring approximately 1-2 mm in length is chosen. The husks and silks are removed and then the ear is broken into halves and placed in an autoclaved solution of Clorox/TWEEN 20 sterilizing solution. Then the ear is rinsed with deionized water. Then each embryo is extracted from the kernel. Intact embryos are placed in contact with the medium, scutellar side up). Multiple embryos are plated on each plate and the plates are incubated in the dark at 25° C. Type II calluses are friable, can be subcultured with a spatula, frequently regenerate via somatic embryogenesis and are relatively undifferentiated. As seen in the microscope, the Tape II calluses show color ranging from translucent to light yellow and heterogeneity on with respect to embryoid structure as well as stage of embryoid development. Once Type II callus are formed, the calluses is transferred to type II callus maintenance medium without AgN0₃. Every 7-10 days, the callus is subcultured. About 4 weeks after embryo isolation the callus is removed from the plates and then frozen in liquid nitrogen. The harvested tissue is stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON021 cDNA library is generated from the immature maize (DK604, Dekalb Genetics, Dekalb Ill., U.S.A.) tassel at the V8 plant development stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the green house in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. As the maize plant enters the V8 stage, tassels which are 15-20 cm in length are collected and frozen in liquid nitrogen. The harvested tissue is stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON022 cDNA library is generated from maize (DK604, Dekalb Genetics, Dekalb, Ill. U.S.A.) ear (growing silks) at the V8 plant development stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the greenhouse in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Tissue is collected when the plant is in the V8 stage. At this stage, some immature ear shoots are visible. The immature ear shoots (approximately 1 cm in length) are pulled out, frozen in liquid nitrogen and then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON23 cDNA library is generated from maize (DK604, Dekalb Genetics, Dekalb, Ill. U.S.A.) ear (growing silk) at the V8 development stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the greenhouse in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. When the tissue is harvested at the V8 stage, the length of the ear that is harvested is about 10-15 cm and the silks are just exposed (approximately 1 inch). The ear along with the silks is frozen in liquid nitrogen and then the tissue is stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON024 cDNA library is generated from the immature maize (DK604, Dekalb Genetics, Dekalb, Ill. U.S.A.) tassel at the V9 development stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the green house in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. As a maize plant enters the V9 stage, the tassel is rapidly developing and a 37 cm tassel along with the glume, anthers and pollen is collected and frozen in liquid nitrogen. The harvested tissue is stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON025 cDNA library is from maize (DK604, Dekalb Genetics, Dekalb, Ill. U.S.A.) Hill Type II-Regenerated Callus. Type II callus is grown in initiation media as described for SATMON020 and then the embryoids on the surface of the Type II callus are allowed to mature and germinate. The 1-2 gm fresh weight of the soft friable type callus containing numerous embryoids are transferred to 100×15 mm petri plates containing 25 ml of regeneration media. Regeneration media consists of Murashige and Skoog (MS) basal salts, modified White's vitamins (0.2 g/liter glycine and 0.5 g/liter myo-inositoland 0.8% bacto agar (6SMS0D)). The plates are then placed in the dark after covering with parafilm. After 1 week, the plates are moved to a lighted growth chamber with 16 hr light and 8 hr dark photoperiod. Three weeks after plating the Type II callus to 6SMS0D, the callus exhibit shoot formation. The callus and the shoots are transferred to fresh 6SMS0D plates for another 2 weeks. The callus and the shoots are then transferred to petri plates with reduced sucrose (3SMSOD). Upon distinct formation of a root and shoot, the newly developed green plants are then removed out with a spatula and frozen in liquid nitrogen containers. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON026 cDNA library is generated from maize (DK604, Dekalb Genetics, Dekalb, Ill. U.S.A.) juvenile/adult shift leaves at the V8 plant development stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the green house in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Tissue is collected when the maize plants are at the 8-leaf development stage. Leaves are founded sequentially around the meristem over weeks of time and the older, more juvenile leaves arise earlier and in a more basal position than the younger, more adult leaves, which are in a more apical position. In a V8 plant, some leaves which are in the middle portion of the plant exhibit characteristics of both juvenile as well as adult leaves. They exhibit a yellowing color but also exhibit, in part, a green color. These leaves are termed juvenile/adult shift leaves. The juvenile/adult shift leaves (the 4th, 5th leaves from the bottom) are cut at the base, pooled and transferred to liquid nitrogen in which they are then crushed. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON027 cDNA library is generated from 6 day maize (DK604, Dekalb Genetics, Dekalb, Ill. U.S.A.) leaves. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the Metro 200 growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the greenhouse in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Prior to tissue collection, when the plant is at the 8-leaf stage, water is held back for six days. The older, more juvenile leaves, which are in a basal position, as well as the younger, more adult leaves, which are more apical, are all cut at the base of the leaves. All the leaves exhibit significant wilting. The leaves are then pooled and immediately transferred to liquid nitrogen containers in which the pooled leaves are then crushed. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON028 cDNA library is generated from maize (DK604, Dekalb Genetics, Dekalb, Ill. U.S.A.) roots at the V8 developmental stage that are subject to six days water stress. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the Metro 200 growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the greenhouse in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Prior to tissue collection, when the plant is at the 8-leaf stage, water is held back for six days. The root system is cut, shaken and washed to remove soil. Root tissue is then pooled and immediately transferred to liquid nitrogen containers in which the pooled leaves are then crushed. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON029 cDNA library is generated from maize (DK604, Dekalb Genetics, Dekalb, Ill. U.S.A.) seedlings at the etiolated stage. Seeds are planted on a moist filter paper on a covered tray that is kept in the dark for 4 days at approximately 70° F. Tissue is collected when the seedlings are 4 days old. By 4 days, the primary root has penetrated the coleorhiza and is about 4-5 cm and the secondary lateral roots have also made their appearance. The coleoptile has also pushed through the seed coat and is about 4-5 cm long. The seedlings are frozen in liquid nitrogen and crushed. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON030 cDNA library is generated from maize (DK604, Dekalb Genetics, Dekalb, Ill. U.S.A.) root tissue at the V4 plant development stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth, they are transplanted into 10 inch pots containing the same. Plants are watered daily before transplantation and approximately 3 times a week after transplantation. Peters 15-16-17 fertilizer is applied approximately three times per week after transplanting, at a strength of 150 ppm N. Two to three times during the life time of the plant, from transplanting to flowering, a total of approximately 900 mg Fe is added to each pot. Maize plants are grown in the green house in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 sodium vapor lamps. Tissue is collected when the maize plant is at the 4 leaf development stage. The root system is cut from the mature maize plant and washed with water to free it from the soil. The tissue is then immediately frozen in liquid nitrogen. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON031 cDNA library is generated from the maize (DK604, Dekalb Genetics, Dekalb, Ill. U.S.A.) leaf tissue at the V4 plant development stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the green house in 15 hr day/9 hr night cycles. The daytime temperature is 80° F. and the nighttime temperature is 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Tissue is collected when the maize plant is at the 4-leaf development stage. The third leaf from the bottom is cut at the base and immediately frozen in liquid nitrogen and crushed. The tissue is immediately frozen in liquid nitrogen. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON033 cDNA library is generated from maize (DK604, Dekalb Genetics, Dekalb, Ill. U.S.A.) embryo tissue 13 days after pollination. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the greenhouse in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. After the V10 stage, the ear shoots of the maize plant, which are ready for fertilization, are enclosed in a paper bag before silk emergent to withhold the pollen. The ear shoots are pollinated and 13 days after pollination, the ears are pulled out and then the kernels are plucked cut of the ears. Each kernel is then dissected into the embryo and the endosperm and the aleurone layer is removed. After dissection, the embryos are immediately frozen in liquid nitrogen and then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON034 cDNA library is generated from cold stressed maize (DK604, Dekalb Genetics, Dekalb, Ill. U.S.A.) seedlings. Seeds are planted on a moist filter paper on a covered tray that is kept on at 10° C. for 7 days. After 7 days, the temperature is shifted to 15° C. for one day until germination of the seed. Tissue is collected once the seedlings are 1 day old. At this point, the coleorhiza has just pushed out of the seed coat and the primary root is just making its appearance. The coleoptile has not yet pushed completely through the seed coat and is also just making its appearance. These 1 day old cold stressed seedlings are frozen in liquid nitrogen and crushed. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMON˜001 (Lib36, Lib83, Lib84) cDNA library is generated from maize leaves at the V8 plant development stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in a greenhouse in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Tissue from the maize plant is collected at the V8 stage. The older more juvenile leaves in a basal position was well as the younger more adult leaves which are more apical are all cut at the base, pooled and frozen in liquid nitrogen. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SATMONN01 cDNA library is generated from maize (B73, Illinois Foundation Seeds, Champaign, Ill. U.S.A.) normalized immature tassels at the V6 plant development stage normalized tissue. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in a greenhouse in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Tissue from the maize plant is collected at the V6 stage. At that stage the tassel is an immature tassel of about 2-3 cm in length. The tassels are removed and frozen in liquid nitrogen. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the normalized cDNA library is constructed as described in Example 2.

The SATMONN04 cDNA library is generated from maize (B73x Mo17, Illinois Foundation Seeds, Champaign, Ill. U.S.A.) normalized total leaf tissue at the V6 plant development stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the greenhouse in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Tissue is collected when the maize plant is at the 6-leaf development stage. The older, more juvenile leaves, which are in a basal position, as well as the younger, more adult leaves, which are more apical are cut at the base of the leaves. The leaves are then pooled and immediately transferred to liquid nitrogen containers in which the pooled leaves are crushed. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the normalized cDNA library is constructed as described in Example 2.

The SATMONN05 cDNA library is generated from maize (B73x Mo17, Illinois Foundation Seeds, Champaign Ill., U.S.A.) normalized root tissue at the V6 development stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the green house in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Tissue is collected when the maize plant is at the 6-leaf development stage. The root system is cut from the mature maize plant and washed with water to free it from the soil. The tissue is immediately frozen in liquid nitrogen and the harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the normalized cDNA library is constructed as described in Example 2.

The SATMONN06 cDNA library is generated from maize (B73x Mo17, Illinois Foundation Seeds, Champaign Ill., U.S.A.) normalized total leaf tissue at the V6 plant development stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the greenhouse in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Tissue is collected when the maize plant is at the 6-leaf development stage. The older more juvenile leaves, which are in a basal position, as well as the younger more adult leaves, which are more apical are cut at the base of the leaves. The leaves are then pooled and immediately transferred to liquid nitrogen containers in which the pooled leaves are crushed. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the normalized cDNA library is constructed as described in Example 2.

The CMZ029 (SATMON036) cDNA library is generated from maize (DK604, Dekalb Genetics, Dekalb, Ill. U.S.A.) endosperm 22 days after pollination. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the green house in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. After the V10 stage, the ear shoots of the maize plant, which are ready for fertilization, are enclosed in a paper bag before silk emergent to withhold the pollen. The ear shoots are pollinated and 22 days after pollination, the ears are pulled out and then the kernels are plucked out of the ears. Each kernel is then dissected into the embryo and the endosperm and the alurone layer is removed. After dissection, the endosperms are immediately frozen in liquid nitrogen and then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The CMz030 (Lib143) cDNA library is generated from maize seedling tissue two days post germination. Seeds are planted on a moist filter paper on a covered try that is keep in the dark until germination. The trays are then moved to the bench top at 15 hr daytime/9 hr nighttime cycles for 2 days post-germination. The day time temperature is 80° F. and the nighttime temperature is 70° F. Tissue is collected when the seedlings are 2 days old. At this stage, the colehrhiza has pushed through the seed coat and the primary root (the radicle) is just piercing the colehrhiza and is barely visible. The seedlings are placed at 42° C. for 1 hour. Following the heat shock treatment, the seedlings are immersed in liquid nitrogen and crushed. The harvested tissue is stored at −80° until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The CMz031 (Lib148) cDNA library is generated from maize pollen tissue at the V10+ plant development stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the greenhouse in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Tissue is collected from V10+ stage plants. The ear shoots, which are ready for fertilization, are enclosed in a paper bag to withhold pollen. Twenty-one days after pollination, prior to removing the ears, the paper bag is shaken to collect the mature pollen. The mature pollen is immediately frozen in liquid nitrogen containers and the pollen is crushed. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The CMz033 (Lib189) cDNA library is generated from maize pooled leaf tissue. Samples are harvested from open pollinated plants. Tissue is collected from maize leaves at the anthesis stage. The leaves are collect from 10-12 plants and frozen in liquid nitrogen. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The CMz034 (Lib3060) cDNA library is generated from maize mature tissue at 40 days post pollination plant development stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the greenhouse in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Tissue is collected from leaves located two leaves below the ear leaf. This sample represents those genes expressed during onset and early stages of leaf senescence. The leaves are pooled and immediately transferred to liquid nitrogen. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The CMz035 (Lib3061) cDNA library is generated from maize endosperm tissue at the V10+ plant development stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the greenhouse in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Tissue is collected from V10+ stage plants. The ear shoots, which are ready for fertilization, are enclosed in a paper bag prior to silk emergence to withhold pollen. Thirty-two days after pollination, the ears are pulled out and the kernels are removed from the cob. Each kernel is dissected into the embryo and the endosperm and the aleurone layer is removed. After dissection, the endosperms are immediately transferred to liquid nitrogen. The harvested tissue is then stored at 80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The CMz036 (Lib3062) cDNA library is generated from maize husk tissue at the 8 week old plant development stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the greenhouse in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Tissue is collected from 8 week old plants. The husk is separated from the ear and immediately transferred to liquid nitrogen containers. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The CMz037 (Lib3059) cDNA library is generated from maize pooled kernel at 12-15 days after pollination plant development stage. Sample were collected from field grown material. Whole kernels from hand pollinated (control pollination) are harvested as whole ears and immediately frozen on dry ice. Kernels from 10-12 ears were pooled and ground together in liquid nitrogen. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The CMz039 (Lib3066) cDNA library is generated from maize immature anther tissue at the 7 week old immature tassel stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the greenhouse in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Tissue is collected when the maize plant is at the 7 week old immature tassel stage. At this stage, prior to anthesis, the immature anthers are green and enclosed in the staminate spikelet. The developing anthers are dissected away from the 7 week old immature tassel and immediately frozen in liquid nitrogen. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The CMz040 (Lib3067) cDNA library is generated from maize kernel tissue at the V10+ plant development stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the greenhouse in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Tissue is collected from V10+ stage plants. The ear shoots, which are ready for fertilization, are enclosed in a paper bag before silk emergence to withhold pollen. Five to eight days after controlled pollination. The ears are pulled and the kernels removed. The kernels are immediately frozen in liquid nitrogen. This sample represents genes expressed in early kernel development, during periods of cell division, amyloplast biogenesis and early carbon flow across the material to filial tissue. The harvested kernels tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The CMz041 (Lib3068) cDNA library is generated from maize pollen germinating silk tissue at the V10+ plant development stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the greenhouse in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Tissue is collected from V10+ stage plants when the ear shoots are ready for fertilization at the silk emergence stage. The emerging silks are pollinated with an excess of pollen under controlled pollination conditions in the green house. Eighteen hours after pollination the silks are removed from the ears and immediately frozen in liquid nitrogen. This sample represents genes expressed in both pollen and silk tissue early in pollination. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The CMz042 (Lib3069) cDNA library is generated from maize ear tissue excessively pollinated at the V10+ plant development stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the greenhouse in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Tissue is collected from VI 0+ stage plants and the ear shoots which are ready for fertilization are at the silk emergence stage. The immature ears are pollinated with an excess of pollen under controlled pollination conditions. Eighteen hours post-pollination, the ears are removed and immediately transferred to liquid nitrogen containers. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The CMz044 (Lib3075) cDNA library is generated from maize microspore tissue at the V10+ plant development stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the greenhouse in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Tissue is collected from immature anthers from 7 week old tassels. The immature anthers are first dissected from the 7 week old tassel with a scalpel on a glass slide covered with water. The microspores (immature pollen) are released into the water and are recovered by centrifugation. The microspore suspension is immediately frozen in liquid nitrogen. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The CMz045 (Lib3076) cDNA library is generated from maize immature ear megaspore tissue. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the greenhouse in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Tissue is collected from immature ear (megaspore) obtained from 7 week old plants. The immature ears are harvested from the 7 week old plants and are approximately 2.5 to 3 cm in length. The kernels are removed from the cob immediately frozen in liquid nitrogen. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The CMz047 (Lib3078) cDNA library is generated from maize CO₂ treated high-exposure shoot tissue at the V10+ plant development stage. RX601 maize seeds are sterilized for i minute with a 10% clorox solution. The seeds are rolled in germination paper, and germinated in 0.5 mM calcium sulfate solution for two days at 30° C. The seedlings are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium at a rate of 2-3 seedlings per pot. Twenty pots are placed into a high CO₂ environment (approximately 1000 ppm CO₂). Twenty plants were grown under ambient greenhouse CO₂ (approximately 450 ppm CO₂). Plants are watered daily before transplantation and three times a week after transplantation. Peters 20-20-20 fertilizer is also lightly applied. Maize plants are grown in the greenhouse in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. At ten days post planting, the shoots from both atmosphere are frozen in liquid nitrogen and lightly ground. The roots are washed in deionized water to remove the support media and the tissue is immediately transferred to liquid nitrogen containers. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The CMz048 (Lib3079) cDNA library is generated from maize basal endosperm transfer layer tissue at the V10+ plant development stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the greenhouse in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Tissue is collected from V10+ maize plants. The ear shoots, which are ready for fertilization, are enclosed in a paper bag prior to silk emergence, to withhold the pollen. Kernels are harvested at 12 days post-pollination and placed on wet ice for dissection. The kernels are cross sectioned laterally, dissecting just above the pedicel region, including 1-2 mm of the lower endosperm and the basal endosperm transfer region. The pedicel and lower endosperm region containing the basal endosperm transfer layer is pooled and immediately frozen in liquid nitrogen. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The CMz049 (Lib3088) cDNA library is generated from maize immature anther tissue at the 7 week old immature tassel stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the greenhouse in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Tissue is collected when the maize plant is at the 7 week old immature tassel stage. At this stage, prior to anthesis, the immature anthers are green and enclosed in the staminate spikelet. The developing anthers are dissected away from the 7 week old immature tassel and immediately transferred to liquid nitrogen container. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The CMz050 (Lib3114) cDNA library is generated from maize silk tissue at the V10+ plant development stage. Seeds are planted at a depth of approximately 3 cm into 2-3 inch peat pots containing Metro 200 growing medium. After 2-3 weeks growth they are transplanted into 10 inch pots containing the same growing medium. Plants are watered daily before transplantation and three times a week after transplantation. Peters 15-16-17 fertilizer is applied three times per week after transplanting at a strength of 150 ppm N. Two to three times during the lifetime of the plant, from transplanting to flowering, a total of 900 mg Fe is added to each pot. Maize plants are grown in the greenhouse in 15 hr day/9 hr night cycles. The daytime temperature is approximately 80° F. and the nighttime temperature is approximately 70° F. Supplemental lighting is provided by 1000 W sodium vapor lamps. Tissue is collected when the maize plant is beyond the 10-leaf development stage and the ear shoots are approximately 15-20 cm in length. The ears are pulled and silks are separated from the ears and immediately transferred to liquid nitrogen containers. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON001 cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) total leaf tissue at the V4 plant development stage. Leaf tissue from 38, field grown V4 stage plants is harvested from the 4^(th) node. Leaf tissue is removed from the plants and immediately frozen in dry-ice. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON002 cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) root tissue at the V4 plant development stage. Root tissue from 76, field grown V4 stage plants is harvested. The root systems is cut from the soybean plant and washed with water to free it from the soil and immediately frozen in dry-ice. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON003 cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) seedling hypocotyl axis tissue harvested 2 day post-imbibition. Seeds are planted at a depth of approximately 2 cm into 2-3 inch peat pots containing Metromix 350 medium. Trays are placed in an environmental chamber and grown at 12 hr daytime/12 hr nighttime cycles. The daytime temperature is approximately 29° C. and the nighttime temperature approximately 24° C. Soil is checked and watered daily to maintain even moisture conditions. Tissue is collected 2 days after the start of imbibition. The 2 days after imbibition samples are separated into 3 collections after removal of any adhering seed coat. At the 2 day stage, the hypocotyl axis is emerging from the soil. A few seedlings have cracked the soil surface and exhibited slight greening of the exposed cotyledons. The seedlings are washed in water to remove soil, hypocotyl axis harvested and immediately frozen in liquid nitrogen. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON004 cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) seedling cotyledon tissue harvested 2 day post-imbibition. Seeds are planted at a depth of approximately 2 cm into 2-3 inch peat pots containing Metromix 350 medium. Trays are placed in an environmental chamber and grown at 12 hr daytime/12 hr nighttime cycles. The daytime temperature is approximately 29° C. and the nighttime temperature approximately 24° C. Soil is checked and watered daily to maintain even moisture conditions. Tissue is collected 2 days after the start of imbibition. The 2 days after imbibition samples are separated into 3 collections after removal of any adhering seed coat. At the 2 day stage, the hypocotyl axis is emerging from the soil. A few seedlings have cracked the soil surface and exhibited slight greening of the exposed cotyledons. The seedlings are washed in water to remove soil, hypocotyl axis harvested and immediately frozen in liquid nitrogen. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON005 cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) seedling hypocotyl axis tissue harvested 6 hour post-imbibition. Seeds are planted at a depth of approximately 2 cm into 2-3 inch peat pots containing Metromix 350 medium. Trays are placed in an environmental chamber and grown at 12 hr daytime/12 hr nighttime cycles. The daytime temperature is approximately 29° C. and the nighttime temperature approximately 24° C. Soil is checked and watered daily to maintain even moisture conditions. Tissue is collected 6 hours after the start of imbibition. The 6 hours after imbibition samples are separated into 3 collections after removal of any adhering seed coat. The 6 hours after imbibition sample is collected over the course of approximately 2 hours starting at 6 hours post imbibition. At the 6 hours after imbibition stage, not all cotyledons have become fully hydrated and germination, or radicle protrusion, has not occurred. The seedlings are washed in water to remove soil, hypocotyl axis harvested and immediately frozen in liquid nitrogen. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON006 cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) seedling cotyledons tissue harvest 6 hour post-imbibition. Seeds are planted at a depth of approximately 2 cm into 2-3 inch peat pots containing Metromix 350 medium. Trays are placed in an environmental chamber and grown at 12 hr daytime/12 hr nighttime cycles. The daytime temperature is approximately 29° C. and the nighttime temperature approximately 24° C. Soil is checked and watered daily to maintain even moisture conditions. Tissue is collected 6 hours after imbibition. The 6 hours after imbibition samples are separated into 3 collections after removal of any adhering seed coat. The 6 hours after imbibition sample is collected over the course of approximately 2 hours starting at 6 hours post-imbibition. At the 6 hours after imbibition, not all cotyledons have become fully hydrated and germination or radicle protrusion, have not occurred. The seedlings are washed in water to remove soil, cotyledon harvested and immediately frozen in liquid nitrogen. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON007 cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) seed tissue harvested 25 and 35 days post-flowering. Seed pods from field grown plants are harvested 25 and 35 days after flowering and the seeds extracted from the pods. Approximately 4.4 g and 19.3 g of seeds are harvested from the respective seed pods and immediately frozen in dry ice. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON008 cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) leaf tissue harvested from 25 and 35 days post-flowering plants. Total leaf tissue is harvested from field grown plants. Approximately 19 g and 29 g of leaves are harvested from the fourth node of the plant 25 and 35 days post-flowering and immediately frozen in dry ice. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON009 cDNA library is generated from soybean cultivar C1944 (USDA Soybean Germplasm Collection, Urbana, Ill. U.S.A.) pod and seed tissue harvested 15 days post-flowering. Pods from field grown plants are harvested 15 days post-flowering. Approximately 3 g of pod tissue is harvested and immediately frozen in dry-ice. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON011 cDNA library is generated from soybean cultivar C1944 (USDA Soybean Germplasm Collection, Urbana, Ill. U.S.A.) seed tissue harvested 40 days post-flowering. Pods from field grown plants are harvested 40 days post-flowering. Pods and seeds are separated, approximately 19 g of seed tissue is harvested and immediately frozen in dry-ice. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON011 cDNA library is generated from soybean cultivars Cristalina (USDA Soybean Germplasm Collection, Urbana, Ill. U.S.A.) and FT108 (Monsoy, Brazil) (tropical germ plasma) leaf tissue. Leaves are harvested from plants grown in an environmental chamber under 12 hr daytime/12 hr nighttime cycles. The daytime temperature is approximately 29° C. and the nighttime temperature approximately 24° C. Soil is checked and watered daily to maintain even moisture conditions. Approximately 30 g of leaves are harvested from the 4^(th) node of each of the Cristalina and FT108 cultivars and immediately frozen in dry ice. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON012 cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) leaf tissue. Leaves from field grown plants are harvested from the fourth node 15 days post-flowering. Approximately 12 g of leaves are harvested and immediately frozen in dry ice. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON013 cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) root and nodule tissue. Approximately, 28 g of root tissue from field grown plants is harvested 15 days post-flowering. The root system is cut from the soybean plant, washed with water to free it from the soil and immediately frozen in dry-ice. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON014 cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) seed tissue harvested 25 and 35 days after flowering. Seed pods from field grown plants are harvested 15 days after flowering and the seeds extracted from the pods. Approximately 5 g of seeds are harvested from the respective seed pods and immediately frozen in dry ice. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON015 cDNA is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) seed tissue harvested 45 and 55 days post-flowering. Seed pods from field grown plants are harvested 45 and 55 days after flowering and the seeds extracted from the pods. Approximately 19 g and 31 g of seeds are harvested from the respective seed pods and immediately frozen in dry ice. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON016 cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) root tissue. Approximately, 61 g and 38 g of root tissue from field grown plants is harvested 25 and 35 days post-flowering is harvested. The root system is cut from the soybean plant and washed with water to free it from the soil. The tissue is placed in 14 ml polystyrene tubes and immediately frozen in dry-ice. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON017 cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) root tissue. Approximately 28 g of root tissue from field grown plants is harvested 45 and 55 days post-flowering. The root system is cut from the soybean plant, washed with water to free it from the soil and immediately frozen in dry-ice. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON018 cDNA is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) leaf tissue harvested 45 and 55 days post-flowering. Leaves from field grown plants are harvested 45 and 55 days after flowering from the fourth node. Approximately 27 g and 33 g of seeds are harvested from the respective seed pods and immediately frozen in dry ice. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON019 cDNA library is generated from soybean cultivars Cristalina (USDA Soybean Germplasm Collection, Urbana, Ill. U.S.A.) and FT108 (Monsoy, Brazil) (tropical germ plasma) root tissue. Roots are harvested from plants grown in an environmental chamber under 12 hr daytime/12 hr nighttime cycles. The daytime temperature is approximately 29° C. and the nighttime temperature approximately 24° C. Soil is checked and watered daily to maintain even moisture conditions. Approximately 50 g and 56 g of roots are harvested from each of the Cristalina and FT108 cultivars and immediately frozen in dry ice. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON020 cDNA is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) seed tissue harvested 65 and 75 days post-flowering. Seed pods from field grown plants are harvested 45 and 55 days after flowering and the seeds extracted from the pods. Approximately 14 g and 31 g of seeds are harvested from the respective seed pods and immediately frozen in dry ice. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON021 cDNA library is generated from Soybean Cyst Nematode-resistant soybean cultivar Hartwig (USDA Soybean Germplasm Collection, Urbana, Ill. U.S.A.) root tissue. Plants are grown in tissue culture at room temperature. At approximately 6 weeks post-germination, the plants are exposed to sterilized Soybean Cyst Nematode eggs. Infection is then allowed to progress for 10 days. After the 10 day infection process, the tissue is harvested. Agar from the culture medium and nematodes are removed and the root tissue is immediately frozen in dry ice. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON022 (Lib3030) cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) partially opened flower tissue. Partially to fully opened flower tissue is harvested from plants grown in an environmental chamber under 12 hr daytime/12 hr nighttime cycles. The daytime temperature is approximately 29° C. and the nighttime temperature approximately 24° C. Soil is checked and watered daily to maintain even moisture conditions. A total of 3 g of flower tissue is harvested and immediately frozen in dry ice. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON023 cDNA library is generated from soybean genotype BW211S Null (Tohoku University, Morioka, Japan) seed tissue harvested 15 and 40 days post-flowering. Seed pods from field grown plants are harvested 15 and 40 days post-flowering and the seeds extracted from the pods. Approximately 0.7 g and 14.2 g of seeds are harvested from the respective seed pods and immediately frozen in dry ice. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON024 cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) internode-2 tissue harvested 18 days post-imbibition. Seeds are planted at a depth of approximately 2 cm into 2-3 inch peat pots containing Metromix 350 medium. The plants are grown in a greenhouse for 18 days after the start of imbibition at ambient temperature. Soil is checked and watered daily to maintain even moisture conditions. Stem tissue is harvested 18 days after the start of imbibition. The samples are divided into hypocotyl and internodes 1 through 5. The fifth internode contains some leaf bud material. Approximately 3 g of each sample is harvested and immediately frozen in dry ice. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON025 cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) leaf tissue harvested 65 days post-flowering. Leaves are harvested from the fourth node of field grown plants 65 days post-flowering. Approximately 18.4 g of leaf tissue is harvested and immediately frozen in dry ice. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

SOYMON026 cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) root tissue harvested 65 and 75 days post-flowering. Approximately 27 g and 40 g of root tissue from field grown plants is harvested 65 and 75 days post-flowering. The root system is cut from the soybean plant, washed with water to free it from the soil and immediately frozen in dry-ice. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON027 cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) pod tissue, without seeds, harvested 25 days post-flowering. Seed pods from field grown plants are harvested 25 days post-flowering and the seeds extracted from the pods. Approximately 17 g of seed pod tissue is harvested and immediately frozen in dry ice. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON028 cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) drought-stressed root tissue. The plants are grown in an environmental chamber under 12 hr daytime/12 hr nighttime cycles. The daytime temperature is approximately 29° C. and the nighttime temperature 24° C. Soil is checked and watered daily to maintain even moisture conditions. At the R3 stage of development, water is withheld from half of the plant collection (drought stressed population). After 3 days, half of the plants from the drought stressed condition and half of the plants from the control population are harvested. After another 3 days (6 days post drought induction) the remaining plants are harvested. A total of 27 g and 40 g of root tissue is harvested and immediately frozen in dry ice. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON029 cDNA library is generated from Soybean Cyst Nematode-resistant soybean cultivar PI07354 (USDA Soybean Germplasm Collection, Urbana, Ill. U.S.A.) root tissue. Late fall to early winter greenhouse grown plants are exposed to Soybean Cyst Nematode eggs. At 10 days post-infection, the plants are uprooted, rinsed briefly and the roots frozen in liquid nitrogen. Approximately 20 grams of root tissue is harvested from the infected plants. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON030 cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) flower bud tissue. Seeds are planted at a depth of approximately 2 cm into 2-3 inch peat pots containing Metromix 350 medium and the plants are grown in an environmental chamber under 12 hr daytime/12 hr nighttime cycles. The daytime temperature is approximately 29° C. and the nighttime temperature approximately 24° C. Soil is checked and watered daily to maintain even moisture conditions. Flower buds are removed from the plant at the pedicel. A total of 100 mg of flower buds are harvested and immediately frozen in liquid nitrogen. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON031 cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) carpel and stamen tissue. Seeds are planted at a depth of approximately 2 cm into 2-3 inch peat pots containing Metromix 350 medium and the plants are grown in an environmental chamber under 12 hr daytime/12 hr nighttime cycles. The daytime temperature is approximately 29° C. and the nighttime temperature approximately 24° C. Soil is checked and watered daily to maintain even moisture conditions. Flower buds are removed from the plant at the pedicel. Flowers are dissected to separate petals, sepals and reproductive structures (carpels and stamens). A total of 300 mg of carpel and stamen tissue are harvested and immediately frozen in liquid nitrogen. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON032 cDNA library is prepared from the Asgrow cultivar A4922 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) rehydrated dry soybean seed meristem tissue. Surface sterilized seeds are germinated in liquid media for 24 hours. The seed axis is then excised from the barely germinating seed, placed on tissue culture media and incubated overnight at 20° C. in the dark. The supportive tissue is removed from the explant prior to harvest. Approximately 570 mg of tissue is harvested and frozen in liquid nitrogen. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON033 cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) heat-shocked seedling tissue without cotyledons. Seeds are imbibed and germinated in vermiculite for 2 days under constant illumination. After 48 hours, the seedlings are transferred to an incubator set at 40° C. under constant illumination. After 30, 60 and 180 minutes seedlings are harvested and dissected. A portion of the seedling consisting of the root, hypocotyl and apical hook is frozen in liquid nitrogen and stored at −80° C. The seedlings after 2 days of imbibition are beginning to emerge from the vermiculite surface. The apical hooks are dark green in appearance. Total RNA and poly A⁺ RNA is prepared from equal amounts of pooled tissue. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON034 cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) cold-shocked seedling tissue without cotyledons. Seeds are imbibed and germinated in vermiculite for 2 days under constant illumination. After 48 hours, the seedlings are transferred to a cold room set at 5° C. under constant illumination. After 30, 60 and 180 minutes seedlings are harvested and dissected. The seedlings after 2 days of imbibition are beginning to emerge from the vermiculite surface. The apical hooks are dark green in appearance. A portion of the seedling consisting of the root, hypocotyl and apical hook is frozen in liquid nitrogen and stored at −80° C. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON035 cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) seed coat tissue. Seeds are planted at a depth of approximately 2 cm into 2-3 inch peat pots containing Metromix 350 medium and the plants are grown in an environmental chamber under 12 hr daytime/12 hr nighttime cycles. The daytime temperature is approximately 29° C. and the nighttime temperature 24° C. Soil is checked and watered daily to maintain even moisture conditions. Seeds are harvested from mid to nearly full maturation (seed coats are not yellowing). The entire embryo proper is removed from the seed coat sample and the seed coat tissue are harvested and immediately frozen in liquid nitrogen. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON036 cDNA library is generated from soybean cultivars PI171451, PI227687 and PI229358 (USDA Soybean Germplasm Collection, Urbana, Ill. U.S.A.) insect challenged leaves. Plants from each of the three cultivars are grown in screenhouse conditions. The screenhouse is divided in half and one half of the screenhouse is infested with soybean looper and the other half infested with velvetbean caterpillar. A single leaf is taken from each of the representative plants at 3 different time points, 11 days after infestation, 2 weeks after infestation and 5 weeks after infestation and immediately frozen in liquid nitrogen. The harvested tissue is then stored at −80° C. until RNA preparation. Total RNA and poly A+ RNA is isolated from pooled tissue consisting of equal quantities of all 18 samples (3 genotypes X3 sample times X2 insect genotypes). The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON037 cDNA library is generated from soybean cultivar A3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) etiolated axis and radical tissue. Seeds are planted in moist vermiculite, wrapped and kept at room temperature in complete darkness until harvest. Etiolated axis and hypocotyl tissue is harvested at 2, 3 and 4 days post-planting. A total of 1 gram of each tissue type is harvested at 2, 3 and 4 days after planting and immediately frozen in liquid nitrogen. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The SOYMON038 cDNA library is generated from soybean variety Asgrow A3237 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) rehydrated dry seeds. Explants are prepared for transformation after germination of surface-sterilized seeds on solid tissue media. After 6 days, at 28° C. and 18 hours of light per day, the germinated seeds are cold shocked at 4° C. for 24 hours. Meristemic tissue and part of the hypocotyl is remove and cotyledon excised. The prepared explant is then wounded for Agrobacterium infection. The 2 grams of harvested tissue is frozen in liquid nitrogen and stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The Soy51 (LIB3027) normalized seed pool cDNA library is prepared from equal amounts tissue harvested from SOYMON007, SOYMON015 and SOYMON020 prepared tissue. Single stranded and double stranded DNA representing approximately 1×10⁶ colony forming units are isolated using standard protocols. RNA, complementary to the single stranded DNA, is synthesized using the double stranded DNA as a template. Biotinylated dATP is incorporated into the RNA during the synthesis reaction. The single stranded DNA is mixed with the biotinylated RNA in a 1:10 molar ratio and allowed to hybridize. DNA-RNA hybrids are captured on Dynabeads M280 streptavidin (Dynabeads, Dynal Corporation, Lake Success, N.Y. U.S.A.). The dynabeads with captured hybrids are collected with a magnet. The non-hybridized single stranded molecules remaining after hybrid capture are converted to double stranded form and represent the primary normalized library.

The Soy52 (LIB3028) cDNA library is generated from normalized flower DNA. Single stranded DNA representing approximately 1×10⁶ colony forming units of SOYMON022 harvested tissue is used as the starting material for normalization. RNA, complementary to the single stranded DNA, is synthesized using the double stranded DNA as a template. Biotinylated dATP is incorporated into the RNA during the synthesis reaction. The single stranded DNA is mixed with the biotinylated RNA in a 1:10 molar ratio and allowed to hybridize. DNA-RNA hybrids are captured on Dynabeads M280 streptavidin (Dynabeads, Dynal Corporation, Lake Success, N.Y. U.S.A.). The dynabeads with captured hybrids are collected with a magnet. The non-hybridized single stranded molecules remaining after hybrid capture are converted to double stranded form and represent the primary normalized library.

The Soy53 (LIB3039) cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) seedling shoot apical meristem tissue. Seeds are planted at a depth of approximately 2 cm into 2-3 inch peat pots containing Metromix 350 medium and the plants are grown in an environmental chamber under 12 hr daytime/12 hr nighttime cycles. The daytime temperature is approximately 29° C. and the nighttime temperature 24° C. Soil is checked and watered daily to maintain even moisture conditions. Apical tissue is harvested from seedling shoot meristem tissue, 7-8 days after the start of imbibition. The apex of each seedling is dissected to include the fifth node to the apical meristem. The fifth node corresponds to the third trifoliate leaf in the very early stages of development. Stipules completely envelop the leaf primordia at this time. A total of 200 mg of apical tissue is harvested and immediately frozen in liquid nitrogen. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

The Soy54 (LIB3040) cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) heart to torpedo stage embryo tissue. Seeds are planted at a depth of approximately 2 cm into 2-3 inch peat pots containing Metromix 350 medium and the plants are grown in an environmental chamber under 12 hr daytime/12 hr nighttime cycles. The daytime temperature is approximately 29° C. and the nighttime temperature 24° C. Soil is checked and watered daily to maintain even moisture conditions. Seeds are collected and embryos removed from surrounding endosperm and maternal tissues. Embryos from globular to young torpedo stages (by corresponding analogy to Arabidopsis) are collected with a bias towards the middle of this spectrum. Embryos which are beginning to show asymmetric development of cotyledons are considered the upper developmental boundary for the collection and are excluded. A total of 12 mg embryo tissue is frozen in liquid nitrogen. The harvested tissue is stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

Soy55 (LIB3049) cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) young seed tissue. Seeds are planted at a depth of approximately 2 cm into 2-3 inch peat pots containing Metromix 350 medium and the plants are grown in an environmental chamber under 12 hr daytime/12 hr nighttime cycles. The daytime temperature is approximately 29° C. and the nighttime temperature 24° C. Soil is checked and watered daily to maintain even moisture conditions. Seeds are collected from very young pods (5 to 15 days after flowering). A total of 100 mg of seeds are harvested and frozen in liquid nitrogen. The harvested tissue is stored at −80° C. until RNA preparation. The RNA is purified from the stored tissue and the cDNA library is constructed as described in Example 2.

Soy56 (LIB3029) non-normalized seed pool cDNA library is prepared from equal amounts tissue harvested from SOYMON007, SOYMON015 and SOYMON020 prepared tissue. Single stranded and double stranded DNA representing approximately 1×10⁶ colony forming units are isolated using standard protocols. RNA, complementary to the single stranded DNA, is synthesized using the double stranded DNA as a template. Biotinylated dATP is incorporated into the RNA during the synthesis reaction. The single stranded DNA is mixed with the biotinylated RNA in a 1:10 molar ratio and allowed to hybridize. DNA-RNA hybrids are captured on Dynabeads M280 streptavidin (Dynabeads, Dynal Corporation, Lake Success, N.Y. U.S.A.). The dynabeads with captured hybrids are collected with a magnet. The non-hybridized single stranded molecules remaining after hybrid capture are not converted to double stranded form and represent a non-normalized seed pool for comparison to Soy51 cDNA libraries.

The Soy58 (LIB3050) cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) drought stressed root tissue subtracted from control root tissue. Seeds are planted at a depth of approximately 2 cm into 2-3 inch peat pots containing Metromix 350 medium and the plants are grown in an environmental chamber under 12 hr daytime/12 hr nighttime cycles. The daytime temperature is approximately 29° C. and the nighttime temperature 24° C. Soil is checked and watered daily to maintain even moisture conditions. At the R3 stage of the plant drought is induced by withholding water. After 3 and 6 days root tissue from both drought stressed and control (watered regularly) plants are collected and frozen in dry-ice. The harvested tissue is stored at −80° C. until RNA preparation. The RNA is prepared from the stored tissue and the subtracted cDNA library is constructed as described in Example 2.

The Soy59 (LIB3051) cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) endosperm tissue. Seeds are germinated on paper towels under laboratory ambient light conditions. At 8, 10 and 14 hours after imbibition, the seed coats are harvested. The endosperm consists of a very thin layer of tissue affixed to the inside of the seed coat. The seed coat and endosperm are frozen immediately after harvest in liquid nitrogen. The harvested tissue is stored at −80° C. until RNA preparation. The RNA is prepared from the stored tissue and the cDNA library is constructed as described in Example 2.

The Soy60 (LIB3072) cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) drought stressed seed plus pod subtracted from control seed plus pod tissue. Seeds are planted at a depth of approximately 2 cm into 2-3 inch peat pots containing Metromix 350 medium and the plants are grown in an environmental chamber under 12 hr daytime/12 hr nighttime cycles. The daytime temperature is approximately 26° C. and the nighttime temperature 21° C. and 70% relative humidity. Soil is checked and watered daily to maintain even moisture conditions. At the R3 stage of the plant drought is induced by withholding water. After 3 and 6 days seeds and pods from both drought stressed and control (watered regularly) plants are collected from the fifth and sixth node and frozen in dry-ice. The harvested tissue is stored at −80° C. until RNA preparation. The RNA is prepared from the stored tissue and the subtracted cDNA library is constructed as described in Example 2.

The Soy61 (LIB3073) cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) jasmonic acid treated seedling subtracted from control tissue. Seeds are planted at a depth of approximately 2 cm into 2-3 inch peat pots containing Metromix 350 medium and the plants are grown in a greenhouse. The daytime temperature is approximately 29.4° C. and the nighttime temperature 20° C. Soil is checked and watered daily to maintain even moisture conditions. At 9 days post planting, the plantlets are sprayed with either control buffer of 0.1% Tween-20 or jasmonic acid (Sigma J-2500, Sigma, St. Louis, Mo. U.S.A.) at 1 mg/ml in 0.1% Tween-20. Plants are sprayed until runoff and the soil and the stem is socked with the spraying solution. At 18 hours post application of jasmonic acid, the soybean plantlets appear growth retarded. After 18 hours, 24 hours and 48 hours post treatment, the cotyledons are removed and the remaining leaf and stem tissue above the soil is harvested and frozen in liquid nitrogen. The harvested tissue is stored at −80° C. until RNA preparation. To make RNA, the three sample timepoints were combined and ground. The RNA is prepared from the stored tissue and the subtracted cDNA library is constructed as described in Example 2. For this library's construction, the eighth fraction of the cDNA size fractionation step was used for ligation.

The Soy62 (LIB3074) cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) jasmonic acid treated seedling subtracted from control tissue. Seeds are planted at a depth of approximately 2 cm into 2-3 inch peat pots containing Metromix 350 medium and the plants are grown in a greenhouse. The daytime temperature is approximately 29.4° C. and the nighttime temperature 20° C. Soil is checked and watered daily to maintain even moisture conditions. At 9 days post planting, the plantlets are sprayed with either control buffer of 0.1% Tween-20 or jasmonic acid (Sigma J-2500, Sigma, St. Louis, Mo. U.S.A.) at 1 mg/ml in 0.1% Tween-20. Plants are sprayed until runoff and the soil and the stem is socked with the spraying solution. At 18 hours post application of jasmonic acid, the soybean plantlets appear growth retarded. After 18 hours, 24 hours and 48 hours post treatment, the cotyledons are removed and the remaining leaf and stem tissue above the soil is harvested and frozen in liquid nitrogen. The harvested tissue is stored at −80° C. until RNA preparation. To make RNA, the three sample timepoints were combined and ground. The RNA is prepared from the stored tissue and the subtracted cDNA library is constructed as described in Example 2. For this library's construction, the ninth fraction of the cDNA size fractionation step was used for ligation.

The Soy65 (LIB3107) 07cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) drought-stressed abscission zone tissue. Seeds are planted at a depth of approximately 2 cm into 2-3 inch peat pots containing Metromix 350 medium and the plants are grown in an environmental chamber under 12 hr daytime/12 hr nighttime cycles. The daytime temperature is approximately 29° C. and the nighttime temperature 24° C. Soil is checked and watered daily to maintain even moisture conditions. Plants are irrigated with 15-16-17 Peter's Mix. At the R3 stage of development, drought is imposed by withholding water. At 3, 4, 5 and 6 days, tissue is harvested and wilting is not obvious until the fourth day. Abscission layers from reproductive organs are harvested by cutting less than one millimeter proximal and distal to the layer and immediately frozen in liquid nitrogen. The harvested tissue is stored at −80° C. until RNA preparation. The RNA is prepared from the stored tissue and the cDNA library is constructed as described in Example 2.

The Soy66 (LIB3109) cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) non-drought stressed abscission zone tissue. Seeds are planted at a depth of approximately 2 cm into 2-3 inch peat pots containing Metromix 350 medium and the plants are grown in an environmental chamber under 12 hr daytime/12 hr nighttime cycles. The daytime temperature is approximately 29° C. and the nighttime temperature approximately 24° C. Soil is checked and watered daily to maintain even moisture conditions. Plants are irrigated with 15-16-17 Peter's Mix. At 3, 4, 5 and 6 days, control abscission layer tissue is harvested. Abscission layers from reproductive organs are harvested by cutting less than one millimeter proximal and distal to the layer and immediately frozen in liquid nitrogen. The harvested tissue is stored at −80° C. until RNA preparation. The RNA is prepared from the stored tissue and the cDNA library is constructed as described in Example 2.

Soy67 (LIB3065) normalized seed pool cDNA library is prepared from equal amounts tissue harvested from SOYMON007, SOYMON015 and SOYMON020 prepared tissue. Single stranded and double stranded DNA representing approximately 1×10⁶ colony forming units are isolated using standard protocols. RNA, complementary to the single stranded DNA, is synthesized using the double stranded DNA as a template. Biotinylated dATP is incorporated into the RNA during the synthesis reaction. The single stranded DNA is mixed with the biotinylated RNA in a 1:10 molar ratio) and allowed to hybridize. DNA-RNA hybrids are captured on Dynabeads M280 streptavidin (Dynabeads, Dynal Corporation, Lake Success, N.Y. U.S.A.). The dynabeads with captured hybrids are collected with a magnet. Captured hybrids are eluted with water.

Soy68 (LIB3052) normalized seed pool cDNA library is prepared from equal amounts tissue harvested from SOYMON007, SOYMON015 and SOYMON020 prepared tissue. Single stranded and double stranded DNA representing approximately 1×10⁶ colony forming units are isolated using standard protocols. RNA, complementary to the single stranded DNA, is synthesized using the double stranded DNA as a template. Biotinylated dATP is incorporated into the RNA during the synthesis reaction. The single stranded DNA is mixed with the biotinylated RNA in a 1:10 molar ratio) and allowed to hybridize. DNA-RNA hybrids are captured on Dynabeads M280 streptavidin (Dynabeads, Dynal Corporation, Lake Success, N.Y. U.S.A.). The dynabeads with captured hybrids are collected with a magnet. Captured hybrids are eluted with water.

Soy69 (LIB3053) normalized cDNA library is generated from soybean cultivars Cristalina (USDA Soybean Germplasm Collection, Urbana, Ill. U.S.A.) and FT108 (Monsoy, Brazil) (tropical germ plasma) normalized leaf tissue. Leaves are harvested from plants grown in an environmental chamber under 12 hr daytime/12 hr nighttime cycles. The daytime temperature is approximately 29° C. and the nighttime temperature approximately 24° C. Soil is checked and watered daily to maintain even moisture conditions. Approximately 30 g of leaves are harvested from the 4^(th) node of each of the Cristalina and FT108 cultivars and immediately frozen in dry ice. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is prepared from the stored tissue and the normalized cDNA library is constructed as described in Example 2.

Soy70 (LIB3055) cDNA library is generated from soybean cultivars Cristalina (USDA Soybean Germplasm Collection, Urbana, Ill. U.S.A.) and FT108 (Monsoy, Brazil) (tropical germ plasma) leaf tissue. Leaves are harvested from plants grown in an environmental chamber under 12 hr daytime/12 hr nighttime cycles. The daytime temperature is approximately 29° C. and the nighttime temperature approximately 24° C. Soil is checked and watered daily to maintain even moisture conditions. Approximately 30 g of leaves are harvested from the 4^(th) node of each of the Cristalina and FT108 cultivars and immediately frozen in dry ice. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is prepared from the stored tissue and the cDNA library is constructed as described in Example 2.

Soy71 (LIB3056) cDNA library is generated from soybean cultivars Cristalina and FT108 (tropical germ plasma) root tissue. Roots are harvested from plants grown in an environmental chamber under 12 hr daytime/12 hr nighttime cycles. The daytime temperature is approximately 29° C. and the nighttime temperature approximately 24° C. Soil is checked and watered daily to maintain even moisture conditions. Approximately 50 g and 56 g of roots are harvested from each of the Cristalina and FT108 cultivars and immediately frozen in dry ice. The harvested tissue is then stored at −80° C. until RNA preparation. The RNA is prepared from the stored tissue and the cDNA library is constructed as described in Example 2.

Soy73 (LIB3093) cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) drought stressed leaf subtracted from control tissue. Seeds are planted at a depth of approximately 2 cm into 2-3 inch peat pots containing Metromix 350 medium and the plants are grown in an environmental chamber under 12 hr daytime/12 hr nighttime cycles. The daytime temperature is approximately 26° C. and the nighttime temperature 21° C. and 70% relative humidity. Soil is checked and watered daily to maintain even moisture conditions. At the R3 stage of the plant drought is induced by withholding water. After 3 and 6 days seeds and pods from both drought stressed and control (watered regularly) plants are collected from the fifth and sixth node and frozen in dry-ice. The harvested tissue is stored at −80° C. until RNA preparation. The RNA is prepared from the stored tissue and the subtraction cDNA library is constructed as described in Example 2.

The Soy76 (Lib3106) cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) jasmonic acid and arachidonic treated seedling subtracted from control tissue. Seeds are planted at a depth of approximately 2 cm into 2-3 inch peat pots containing Metromix 350 medium and the plants are grown in a greenhouse. The daytime temperature is approximately 29.4° C. and the nighttime temperature 20° C. Soil is checked and watered daily to maintain even moisture conditions. At 9 days post planting, the plantlets are sprayed with either control buffer of 0.1% Tween-20 or jasmonic acid (Sigma J-2500, Sigma, St. Louis, Mo. U.S.A.) at 1 mg/ml in 0.1% Tween-20. Plants are sprayed until runoff and the soil and the stem is socked with the spraying solution. At 18 hours post application of jasmonic acid, the soybean plantlets appear growth retarded. Arachidonic treated seedlings are sprayed with 1 m/ml arachidonic acid in 0.1% Tween-20. After 18 hours, 24 hours and 48 hours post treatment, the cotyledons are removed and the remaining leaf and stem tissue above the soil is harvested and frozen in liquid nitrogen. The harvested tissue is stored at −80° C. until RNA preparation. To make RNA, the three sample timepoints were combined and ground. The RNA from the arachidonic treated seedlings is isolated separately. The RNA is prepared from the stored tissue and the subtraction cDNA library is constructed as described in Example 2. For this subtraction library, fraction 10 of the size fractionated cDNA is ligated into the pSPORT vector (Invitrogen, Carlsbad Calif. U.S.A.) in order to capture some of the smaller transcripts characteristic of antifungal proteins.

Soy77 (LIB3108) cDNA library is generated from soybean cultivar Asgrow 3244 (Asgrow Seed Company, Des Moines, Iowa U.S.A.) jasmonic acid control tissue. Seeds are planted at a depth of approximately 2 cm into 2-3 inch peat pots containing Metromix 350 medium and the plants are grown in a greenhouse. The daytime temperature is approximately 29.4° C. and the nighttime temperature 20° C. Soil is checked and watered daily to maintain even moisture conditions. At 9 days post planting, the plantlets are sprayed with either control buffer of 0.1% Tween-20 or jasmonic acid (Sigma J-2500, Sigma, St. Louis, Mo. U.S.A.) at 1 mg/ml in 0.1% Tween-20. Plants are sprayed until runoff and the soil and the stem is socked with the spraying solution. At 18 hours post application of jasmonic acid, the soybean plantlets appear growth retarded. Arachidonic treated seedlings are sprayed with 1 m/ml arachidonic acid in 0.1% Tween-20. After 18 hours, 24 hours and 48 hours post treatment, the cotyledons are removed and the remaining leaf and stem tissue above the soil is harvested and frozen in liquid nitrogen. The harvested tissue is stored at −80° C. until RNA preparation. To make RNA, the three sample timepoints were combined and ground. The RNA from the arachidonic treated seedlings is isolated separately. The RNA is prepared from the stored tissue and the subtraction cDNA library is constructed as described in Example 2. For this subtraction cDNA library, fraction 10 of the size fractionated cDNA is ligated into the pSPORT vector in order to capture some of the smaller transcripts characteristic of antifungal proteins.

EXAMPLE 2

The stored RNA is purified using Trizol reagent from Life Technologies (Gibco BRL, Life Technologies, Gaithersburg, Md. U.S.A.), essentially as recommended by the manufacturer. Poly A+ RNA (mRNA) is purified using magnetic oligo dT beads essentially as recommended by the manufacturer (Dynabeads, Dynal Corporation, Lake Success, N.Y. U.S.A.).

Construction of plant cDNA libraries is well-known in the art and a number of cloning strategies exist. A number of cDNA library construction kits are commercially available. The Superscript™ Plasmid System for cDNA synthesis and Plasmid Cloning (Gibco BRL, Life Technologies, Gaithersburg, Md. U.S.A.) is used, following the conditions suggested by the manufacturer.

Normalized libraries are made using essentially the Soares procedure (Soares et al., Proc. Natl. Acad. Sci. (U.S.A.) 91:9228-9232 (1994), the entirety of which is herein incorporated by reference). This approach is designed to reduce the initial 10,000-fold variation in individual cDNA frequencies to achieve abundances within one order of magnitude while maintaining the overall sequence complexity of the library. In the normalization process, the prevalence of high-abundance cDNA clones decreases dramatically, clones with mid-level abundance are relatively unaffected and clones for rare transcripts are effectively increased in abundance.

Normalized libraries are prepared from single-stranded and double-stranded DNA. Single-stranded and double-stranded DNA representing approximately 1×10⁶ colony forming units are isolated using standard protocols. RNA, complementary to the single-stranded DNA, is synthesized using the double stranded DNA as a template. Biotinylated dATP is incorporated into the RNA during the synthesis reaction. The single-stranded DNA is mixed with the biotinylated RNA in a 1:10 molar ratio) and allowed to hybridize. DNA-RNA hybrids are captured on Dynabeads M280 streptavidin (Dynabeads, Dynal Corporation, Lake Success, N.Y. U.S.A.). The dynabeads with captured hybrids are collected with a magnet. The non-hybridized single-stranded molecules remaining after hybrid capture are converted to double stranded form and represent the primary normalized library.

For subtraction, target cDNA is made from the drought stressed tissue total RNA using the SMART cDNA synthesis system from Clonetech (Clonetech Laboratories, Palo Alto, Calif. U.S.A.). Driver first strand cDNA is covalently linked to Dynabeads following a protocol similar to that described in the Dynal literature (Dynabeads, Dynal Corporation, Lake Success, N.Y. U.S.A.). The target cDNA is then heat denatured and the second strand trapped using Dynabeads oligo-dT. The target second strand cDNA is then hybridized to the driver cDNA in 400 l 2×SSPE for two rounds of hybridization at 65° C. and 20 hours. After each hybridization, the hybridization solution is removed from the system and the hybridized target cDNA removed from the driver by heat denaturation in water. After hybridization, the remaining cDNA is trapped with Dynabeads oligo-dT. The trapped cDNA is then amplified as in previous PCR based libraries and the resulting cDNA ligated into the pSPORT vector (Invitrogen, Carlsbad Calif. U.S.A.).

EXAMPLE 3

The cDNA libraries are plated on LB agar containing the appropriate antibiotics for selection and incubated at 37° for a sufficient time to allow the growth of individual colonies. Single colonies are individually placed in each well of a 96-well microtiter plates containing LB liquid including the selective antibiotics. The plates are incubated overnight at approximately 37° C. with gentle shaking to promote growth of the cultures. The plasmid DNA is isolated from each clone using Qiaprep plasmid isolation kits, using the conditions recommended by the manufacturer (Qiagen Inc., Santa Clara, Calif. U.S.A.).

Template plasmid DNA clones are used for subsequent sequencing. For sequencing, the ABI PRISM dRhodamine Terminator Cycle Sequencing Ready Reaction Kit with AmpliTaq® DNA Polymerase, FS, is used (PE Applied Biosystems, Foster City, Calif. U.S.A.).

EXAMPLE 4

Nucleic acid sequences that encode for the following carbon assimilation pathway enzymes: ribulose-bisphosphate carboxylase, phosphoglycerate kinase, glyceraldehyde 3-phosphate dehydrogenase, putative glyceraldehyde 3-phosphate dehydrogenase, triose phosphate isomerase, aldolase, fructose-1,6-bisphosphatase, transketolase, putative transketolase, sedoheptulose-1,7-bisphosphatase, D-ribulose-5-phosphate-3-epimerase, ribose-5-phosphate isomerase, putative ribose-5-phosphate isomerase, ribose-5-phosphate kinase, phosphoenolpyruvate carboxylase, NADP-dependent malate dehydrogenase, aspartate aminotransferase, putative aspartate aminotransferase, alanine aminotransferase, NADP-dependent malic enzyme, NAD-dependent malic enzyme, PEP carboxykinase, putative PEP carboxykinase, pyruvate, phosphate dikinase and pyrophosphatase are identified from the Monsanto EST PhytoSeq database using TBLASTN (default values) (TBLASTN compares a protein query against the six reading frames of a nucleic acid sequence). Matches found with BLAST P values equal or less than 0.001 (probability) or BLAST Score of equal or greater than 90 are classified as hits. If the program used to determine the hit is HMMSW then the score refers to HMMSW score.

In addition, the GenBank database is searched with BLASTN and BLASTX (default values) using ESTs as queries. EST that pass the hit probability threshold of 10e⁻⁸ for the following enzymes are combined with the hits generated by using TBLASTN (described above) and classified by enzyme (see Table A below).

A cluster refers to a set of overlapping clones in the PhytoSeq database. Such an overlapping relationship among clones is designated as a “cluster” when BLAST scores from pairwise sequence comparisons of the member clones meets a predetermined minimum value or product score of 50 or more (Product Score=(BLAST SCORE×Percentage Identity)/(5×minimum[length(Seq1),length(Seq2)]))

Since clusters are formed on the basis of single-linkage relationships, it is possible for two non-overlapping clones to be members of the same cluster if, for instance, they both overlap a third clone with at least the predetermined minimum BLAST score (stringency). A cluster ID is arbitrarily assigned to all of those clones which belong to the same cluster at a given stringency and a particular clone will belong to only one cluster at a given stringency. If a cluster contains only a single clone (a “singleton”), then the cluster ID number will be negative, with an absolute value equal to the clone ID number of its single member. Clones grouped in a cluster in most cases represent a contiguous sequence.

TABLE A* MAIZE RIBULOSE-BISPHOSPHATE CARBOXYLASE Seq No. Cluster ID Clone ID Library NCBI gi Method Score P-value % Ident 1 -700430856 700430856H1 SATMONN01 g22464 BLASTN 215 1e−9 100 2 21707 700433144H1 SATMONN01 g22464 BLASTN 626 1e−45 95 3 21707 700433148H1 SATMONN01 g22464 BLASTN 626 1e−45 95 4 3272 700098783H1 SATMON009 g217963 BLASTN 1535 1e−128 98 5 3272 700097213H1 SATMON009 g217963 BLASTN 1316 1e−121 99 6 3272 700097673H1 SATMON009 g217963 BLASTN 1540 1e−121 96 7 3272 700101767H1 SATMON009 g1673455 BLASTN 1095 1e−120 100 8 3272 700100001H1 SATMON009 g1673455 BLASTN 910 1e−119 99 9 3272 700097382H1 SATMON009 g217963 BLASTN 1517 1e−119 96 10 3272 700099925H1 SATMON009 g217963 BLASTN 1522 1e−119 97 11 3272 700098235H1 SATMON009 g217963 BLASTN 1512 1e−118 97 12 3272 700093043H1 SATMON008 g1673455 BLASTN 1070 1e−117 100 13 3272 700089802H1 SATMON011 g217963 BLASTN 996 1e−115 95 14 3272 700101196H1 SATMON009 g217963 BLASTN 1478 1e−115 99 15 3272 700097309H1 SATMON009 g217963 BLASTN 1482 1e−115 97 16 3272 700100270H1 SATMON009 g217963 BLASTN 1466 1e−114 96 17 3272 700208152H1 SATMON016 g1673455 BLASTN 1090 1e−113 99 18 3272 700215709H1 SATMON016 g1673455 BLASTN 1105 1e−113 98 19 3272 700100795H1 SATMON009 g217963 BLASTN 1452 1e−113 98 20 3272 700097496H1 SATMON009 g217963 BLASTN 1416 1e−110 99 21 3272 700099783H1 SATMON009 g217963 BLASTN 1427 1e−110 97 22 3272 700044355H1 SATMON004 g217963 BLASTN 1326 1e−109 96 23 3272 700099951H1 SATMON009 g217963 BLASTN 1409 1e−109 96 24 3272 700100228H1 SATMON009 g217963 BLASTN 999 1e−108 97 25 3272 700042150H1 SATMON004 g217963 BLASTN 1186 1e−108 99 26 3272 700045728H1 SATMON004 g217963 BLASTN 1313 1e−108 96 27 3272 700098561H1 SATMON009 g217963 BLASTN 1236 1e−107 96 28 3272 700100271H1 SATMON009 g217963 BLASTN 1392 1e−107 93 29 3272 700211770H1 SATMON016 g217963 BLASTN 1097 1e−105 97 30 3272 700095614H1 SATMON008 g217963 BLASTN 1366 1e−105 91 31 3272 700577012H1 SATMON031 g217963 BLASTN 1348 1e−104 97 32 3272 700100637H1 SATMON009 g217963 BLASTN 1357 1e−104 97 33 3272 700045636H1 SATMON004 g217963 BLASTN 1240 1e−103 100 34 3272 700210942H1 SATMON016 g217963 BLASTN 1183 1e−102 97 35 3272 700213737H1 SATMON016 g217963 BLASTN 1286 1e−102 96 36 3272 700097664H1 SATMON009 g1673455 BLASTN 1093 1e−101 99 37 3272 700212658H1 SATMON016 g217963 BLASTN 1312 1e−101 97 38 3272 700101672H1 SATMON009 g217963 BLASTN 1313 1e−101 97 39 3272 700053379H1 SATMON009 g217963 BLASTN 1315 1e−101 95 40 3272 700025653H1 SATMON004 g217963 BLASTN 1316 1e−101 99 41 3272 700333193H1 SATMON019 g217963 BLASTN 1318 1e−101 97 42 3272 700211830H1 SATMON016 g217963 BLASTN 1042 1e−100 94 43 3272 700097362H1 SATMON009 g217963 BLASTN 1300 1e−100 93 44 3272 700214096H1 SATMON016 g217963 BLASTN 1308 1e−100 97 45 3272 700042186H1 SATMON004 g217963 BLASTN 1287 1e−99 97 46 3272 700097564H1 SATMON009 g217963 BLASTN 1293 1e−99 92 47 3272 700097886H1 SATMON009 g217963 BLASTN 1232 1e−98 97 48 3272 700043286H1 SATMON004 g217963 BLASTN 1281 1e−98 99 49 3272 700356225H1 SATMON024 g217963 BLASTN 881 1e−97 95 50 3272 700046066H1 SATMON004 g1673455 BLASTN 930 1e−97 100 51 3272 700433801H1 SATMONN01 g22464 BLASTN 960 1e−97 99 52 3272 701185535H1 SATMONN06 g22464 BLASTN 1271 1e−97 99 53 3272 700044292H1 SATMON004 g217963 BLASTN 1257 1e−96 97 54 3272 700053495H1 SATMON009 g217963 BLASTN 1261 1e−96 96 55 3272 700053373H1 SATMON009 g217963 BLASTN 1058 1e−95 99 56 3272 700224630H1 SATMON011 g217963 BLASTN 1243 1e−95 99 57 3272 700046049H1 SATMON004 g217963 BLASTN 702 1e−94 92 58 3272 700045078H1 SATMON004 g217963 BLASTN 880 1e−94 100 59 3272 700046107H1 SATMON004 g1673455 BLASTN 940 1e−94 100 60 3272 700045287H1 SATMON004 g217963 BLASTN 975 1e−94 100 61 3272 700210539H1 SATMON016 g217963 BLASTN 1230 1e−94 92 62 3272 700212887H1 SATMON016 g217963 BLASTN 896 1e−93 96 63 3272 700421770H1 SATMONN01 g217963 BLASTN 1226 1e−93 96 64 3272 700211658H1 SATMON016 g217963 BLASTN 800 1e−91 99 65 3272 701182334H1 SATMONN06 g1673455 BLASTN 926 1e−90 98 66 3272 700044245H1 SATMON004 g217963 BLASTN 1190 1e−90 100 67 3272 700045992H1 SATMON004 g1673455 BLASTN 931 1e−89 99 68 3272 700215027H1 SATMON016 g217963 BLASTN 937 1e−89 96 69 3272 700042688H1 SATMON004 g217963 BLASTN 1100 1e−89 97 70 3272 700044947H1 SATMON004 g217963 BLASTN 1175 1e−89 100 71 3272 700045847H1 SATMON004 g217963 BLASTN 1180 1e−89 96 72 3272 700215351H1 SATMON016 g1673455 BLASTN 940 1e−88 100 73 3272 700094920H1 SATMON008 g217963 BLASTN 957 1e−88 91 74 3272 700044201H1 SATMON004 g217963 BLASTN 596 1e−87 100 75 3272 700335684H1 SATMON019 g22464 BLASTN 925 1e−87 94 76 3272 700101503H1 SATMON009 g217963 BLASTN 1108 1e−87 92 77 3272 700099376H1 SATMON009 g1673455 BLASTN 940 1e−85 98 78 3272 700099542H1 SATMON009 g217963 BLASTN 1129 1e−85 91 79 3272 700046244H1 SATMON004 g217963 BLASTN 1112 1e−84 97 80 3272 700088638H1 SATMON011 g217963 BLASTN 1100 1e−83 92 81 3272 700044223H1 SATMON004 g1673455 BLASTN 839 1e−82 96 82 3272 700042573H1 SATMON004 g1673455 BLASTN 839 1e−82 96 83 3272 700214068H1 SATMON016 g1673455 BLASTN 940 1e−82 100 84 3272 700198026H1 SATMON016 g217963 BLASTN 1082 1e−81 96 85 3272 700045910H1 SATMON004 g217963 BLASTN 1085 1e−81 92 86 3272 700097189H1 SATMON009 g217963 BLASTN 1051 1e−79 91 87 3272 700042282H1 SATMON004 g217963 BLASTN 1055 1e−79 93 88 3272 700045136H1 SATMON004 g1673455 BLASTN 832 1e−78 96 89 3272 700097141H1 SATMON009 g217963 BLASTN 1045 1e−78 91 90 3272 700025538H1 SATMON004 g1673455 BLASTN 940 1e−76 99 91 3272 700042620H1 SATMON004 g217963 BLASTN 1001 1e−74 92 92 3272 700042070H1 SATMON004 g217963 BLASTN 890 1e−73 93 93 3272 700218243H1 SATMON016 g217963 BLASTN 896 1e−73 99 94 3272 700043362H1 SATMON004 g217963 BLASTN 970 1e−72 93 95 3272 700043484H1 SATMON004 g217963 BLASTN 945 1e−70 93 96 3272 700042923H1 SATMON004 g217963 BLASTN 445 1e−69 88 97 3272 700441659H1 SATMON026 g217963 BLASTN 703 1e−69 95 98 3272 700044543H1 SATMON004 g217963 BLASTN 940 1e−69 93 99 3272 700214747H1 SATMON016 g217963 BLASTN 925 1e−68 97 100 3272 700084502H1 SATMON011 g217963 BLASTN 721 1e−66 85 101 3272 700046322H1 SATMON004 g217963 BLASTN 893 1e−65 92 102 3272 700216096H1 SATMON016 g1673455 BLASTN 877 1e−64 95 103 3272 700043871H1 SATMON004 g217963 BLASTN 880 1e−64 92 104 3272 700429382H1 SATMONN01 g529673 BLASTN 440 1e−63 92 105 3272 700442416H1 SATMON026 g217963 BLASTN 603 1e−60 88 106 3272 700208826H1 SATMON016 g217963 BLASTN 379 1e−59 98 107 3272 700209462H1 SATMON016 g22464 BLASTN 796 1e−59 95 108 3272 700209449H1 SATMON016 g1673455 BLASTN 609 1e−53 94 109 3272 700354501H1 SATMON024 g217963 BLASTN 644 1e−52 94 110 3272 700099672H1 SATMON009 g22464 BLASTN 648 1e−45 95 111 3272 700216452H1 SATMON016 g529673 BLASTN 550 1e−37 84 112 3272 700097732H1 SATMON009 g1673455 BLASTN 453 1e−28 98 113 3272 700334324H1 SATMON019 g1673455 BLASTN 434 1e−27 97 114 8171 700098206H1 SATMON009 g1673455 BLASTN 711 1e−105 94 115 8171 700443785H1 SATMON027 g1673455 BLASTN 727 1e−97 97 116 8171 700444325H1 SATMON027 g1673455 BLASTN 1091 1e−82 98 117 8171 700096125H1 SATMON008 g1673455 BLASTN 749 1e−64 92 118 8171 700447385H1 SATMON027 g1673455 BLASTN 601 1e−54 88 119 8171 700101184H1 SATMON009 g1673455 BLASTN 613 1e−52 90 120 8171 700042451H1 SATMON004 g1673455 BLASTN 507 1e−43 94 121 -L1892710 LIB189-012- LIB189 g18035 BLASTN 745 1e−53 87 Q1-E1-F5 122 -L1893905 LIB189-022- LIB189 g1040912 BLASTN 1259 1e−96 84 Q1-E1-A5 123 -L30601614 LIB3060-004- LIB3060 g12394 BLASTN 497 1e−47 90 Q1-K1-D4 124 -L30601698 LIB3060-005- LIB3060 g12394 BLASTN 813 1e−82 90 Q1-K1-A3 125 -L30604185 LIB3060-040- LIB3060 g22464 BLASTN 508 1e−46 83 Q1-K1-G6 126 -L30605233 LIB3060-050- LIB3060 g18035 BLASTN 425 1e−43 84 Q1-K1-E5 127 -L30623478 LIB3062-029- LIB3062 g22464 BLASTN 260 1e−27 81 Q1-K1-F9 128 -L30624113 LIB3062-015- LIB3062 g1673455 BLASTN 264 1e−39 83 Q1-K1-E9 129 -L30626076 LIB3062-057- LIB3062 g217963 BLASTN 332 1e−18 85 Q1-K1-G7 130 -L30673250 LIB3067-018- LIB3067 g18035 BLASTN 1123 1e−100 81 Q1-K1-F10 131 -L30681922 LIB3068-020- LIB3068 g1040894 BLASTN 1180 1e−106 86 Q1-K1-A6 132 -L30686213 LIB3068-050- LIB3068 g18035 BLASTN 1402 1e−108 96 Q1-K1-B9 133 -L30686456 LIB3068-016- LIB3068 g11750 BLASTN 337 1e−90 84 Q1-K1-D3 134 -L30781756 LIB3078-015- LIB3078 g1673455 BLASTN 296 1e−31 82 Q1-K1-A3 135 -L30782307 LIB3078-006- LIB3078 g217963 BLASTN 313 1e−17 84 Q1-K1-A3 136 -L30782348 LIB3078-006- LIB3078 g217964 BLASTN 64 1e−26 44 Q1-K1-C8 137 -L30783621 LIB3078-053- LIB3078 g217963 BLASTN 461 1e−39 69 Q1-K1-B1 138 -L30784234 LIB3078-034- LIB3078 g217963 BLASTN 288 1e−30 84 Q1-K1-C1 139 -L30784545 LIB3078-039- LIB3078 g18035 BLASTN 944 1e−96 88 Q1-K1-H12 140 -L361484 LIB36-008- LIB36 g217963 BLASTN 683 1e−58 92 Q1-E1-E1 141 -L361797 LIB36-020- LIB36 g12394 BLASTN 290 1e−32 76 Q1-E1-H9 142 -L362703 LIB36-018- LIB36 g1040892 BLASTN 1253 1e−95 90 Q1-E1-D9 143 -L84236 LIB84-004- LIB84 g217963 BLASTN 322 1e−50 81 Q1-E1-A2 144 -L84828 LIB84-015- LIB84 g18035 BLASTN 473 1e−36 86 Q1-E1-B4 145 24099 LIB36-014- LIB36 g18035 BLASTN 2297 1e−183 99 Q1-E1-C4 146 24099 LIB36-014- LIB36 g18035 BLASTN 2294 1e−182 99 Q1-E1-B6 147 24099 LIB3068-005- LIB3068 g18035 BLASTN 2188 1e−179 93 Q1-K1-B1 148 24099 LIB3066-053- LIB3066 g18035 BLASTN 2252 1e−179 97 Q1-K1-H3 149 24099 LIB36-016- LIB36 g18035 BLASTN 1369 1e−176 99 Q2-E2-F11 150 24099 LIB3068-022- LIB3068 g18035 BLASTN 2209 1e−175 98 Q1-K1-C10 151 24099 LIB3078-007- LIB3078 g18035 BLASTN 2004 1e−172 99 Q1-K1-B11 152 24099 LIB3078-049- LIB3078 g18035 BLASTN 2154 1e−171 98 Q1-K1-A1 153 24099 LIB3060-016- LIB3060 g18035 BLASTN 2151 1e−170 99 Q1-K1-C8 154 24099 LIB189-012- LIB189 g18035 BLASTN 2132 1e−169 98 Q1-E1-F10 155 24099 LIB3078-049- LIB3078 g18035 BLASTN 2136 1e−169 99 Q1-K1-G3 156 24099 LIB3060-025- LIB3060 g18035 BLASTN 1587 1e−167 99 Q1-K1-H1 157 24099 LIB3060-016- LIB3060 g18035 BLASTN 2112 1e−167 98 Q1-K1-D2 158 24099 LIB189-029- LIB189 g18035 BLASTN 1942 1e−166 98 Q1-E1-H11 159 24099 LIB36-021- LIB36 g18035 BLASTN 2096 1e−166 99 Q1-E1-H9 160 24099 LIB84-008- LIB84 g18035 BLASTN 2090 1e−165 100 Q1-E1-G8 161 24099 LIB36-021- LIB36 g18035 BLASTN 1923 1e−164 98 Q1-E1-B7 162 24099 LIB189-016- LIB189 g18035 BLASTN 2070 1e−164 97 Q1-E1-A3 163 24099 LIB3060-052- LIB3060 g18035 BLASTN 1634 1e−163 95 Q1-K1-B5 164 24099 LIB3078-023- LIB3078 g18035 BLASTN 1659 1e−163 95 Q1-K1-F3 165 24099 LIB3066-005- LIB3066 g18035 BLASTN 1819 1e−163 97 Q1-K1-D11 166 24099 LIB189-023- LIB189 g18035 BLASTN 1697 1e−161 96 Q1-E1-H10 167 24099 LIB189-004- LIB189 g18035 BLASTN 1705 1e−161 92 Q1-E1-B6 168 24099 LIB3078-018- LIB3078 g18035 BLASTN 1748 1e−161 98 Q1-K1-F2 169 24099 LIB3066-003- LIB3066 g18035 BLASTN 2034 1e−160 96 Q1-K1-F3 170 24099 LIB3062-053- LIB3062 g18035 BLASTN 1761 1e−159 96 Q1-K1-D2 171 24099 LIB3069-017- LIB3069 g11750 BLASTN 1144 1e−157 95 Q1-K1-E6 172 24099 LIB3078-054- LIB3078 g18035 BLASTN 1980 1e−156 95 Q1-K1-H4 173 24099 LIB3060-036- LIB3060 g18035 BLASTN 1960 1e−154 96 Q1-K1-F5 174 24099 LIB3078-014- LIB3078 g18035 BLASTN 1961 1e−154 99 Q1-K1-E11 175 24099 LIB3066-015- LIB3066 g18035 BLASTN 1526 1e−152 96 Q1-K1-D8 176 24099 LIB3068-016- LIB3068 g18035 BLASTN 1925 1e−151 91 Q1-K1-D2 177 24099 LIB189-011- LIB189 g1040894 BLASTN 1675 1e−150 98 Q1-E1-F8 178 24099 LIB3060-002- LIB3060 g1040894 BLASTN 1578 1e−149 97 Q1-K2-B4 179 24099 LIB3078-004- LIB3078 g1040912 BLASTN 1609 1e−149 94 Q1-K1-G9 180 24099 LIB189-031- LIB189 g18035 BLASTN 1775 1e−149 98 Q1-E1-A5 181 24099 LIB36-019- LIB36 g18035 BLASTN 1718 1e−146 97 Q1-E1-F7 182 24099 LIB84-030- LIB84 g1040894 BLASTN 1822 1e−146 98 Q1-E1-G10 183 24099 LIB3062-031- LIB3062 g18035 BLASTN 791 1e−145 93 Q1-K1-A10 184 24099 LIB3078-014- LIB3078 g18035 BLASTN 1817 1e−142 98 Q1-K1-E2 185 24099 LIB189-020- LIB189 g1040892 BLASTN 1660 1e−140 96 Q1-E1-G2 186 24099 LIB189-003- LIB189 g18035 BLASTN 1774 1e−139 97 Q1-E1-G6 187 24099 LIB3060-009- LIB3060 g18035 BLASTN 1240 1e−138 96 Q1-K1-F8 188 24099 LIB3078-011- LIB3078 g18035 BLASTN 1771 1e−138 91 Q1-K1-C10 189 24099 LIB3066-027- LIB3066 g11750 BLASTN 1289 1e−133 94 Q1-K1-H12 190 24099 LIB84-005- LIB84 g18035 BLASTN 1137 1e−132 96 Q1-E1-B4 191 24099 LIB3078-027- LIB3078 g18035 BLASTN 1450 1e−131 99 Q1-K1-E11 192 24099 LIB36-016- LIB36 g18035 BLASTN 1661 1e−129 99 Q2-E2-G10 193 24099 LIB3060-020- LIB3060 g18035 BLASTN 1334 1e−126 96 Q1-K1-H7 194 24099 LIB3068-045- LIB3068 g11750 BLASTN 1349 1e−126 91 Q1-K1-F6 195 24099 LIB3060-048- LIB3060 g18035 BLASTN 1517 1e−126 90 Q1-K1-C5 196 24099 LIB3078-028- LIB3078 g1040912 BLASTN 1094 1e−125 96 Q1-K1-G7 197 24099 LIB3078-008- LIB3078 g18035 BLASTN 1282 1e−122 83 Q1-K1-F7 198 24099 LIB3078-035- LIB3078 g1040892 BLASTN 1194 1e−118 81 Q1-K1-H4 199 24099 LIB36-015- LIB36 g18035 BLASTN 1508 1e−116 98 Q1-E1-E1 200 24099 LIB3060-029- LIB3060 g1040894 BLASTN 1400 1e−112 95 Q1-K1-E10 201 24099 LIB3060-038- LIB3060 g18035 BLASTN 1356 1e−104 97 Q1-K1-B8 202 24099 LIB189-026- LIB189 g18035 BLASTN 1319 1e−101 93 Q1-E1-D9 203 24099 LIB189-034- LIB189 g18035 BLASTN 748 1e−97 89 Q1-E1-D10 204 24099 LIB189-023- LIB189 g18035 BLASTN 635 1e−86 93 Q1-E1-F3 205 24099 LIB83-001- LIB83 g18035 BLASTN 540 1e−68 99 Q1-E1-E9 206 24099 LIB189-021- LIB189 g18035 BLASTN 715 1e−50 100 Q1-E1-D6 207 24207 LIB3060-026- LIB3060 g11797 BLASTN 694 1e−149 90 Q1-K1-C3 208 24207 LIB189-018- LIB189 g11797 BLASTN 904 1e−143 96 Q1-E1-E9 209 24207 LIB3060-020- LIB3060 g11797 BLASTN 694 1e−115 91 Q1-K1-A10 210 3272 LIB3078-018- LIB3078 g217963 BLASTN 2129 1e−180 97 Q1-K1-H8 211 3272 LIB36-009- LIB36 g217963 BLASTN 2057 1e−178 95 Q1-E1-E12 212 3272 LIB3078-013- LIB3078 g217963 BLASTN 2154 1e−173 99 Q1-K1-H11 213 3272 LIB83-007- LIB83 g217963 BLASTN 2008 1e−172 97 Q1-E1-C9 214 3272 LIB36-014- LIB36 g217963 BLASTN 1905 1e−171 99 Q1-E1-H9 215 3272 LIB3066-002- LIB3066 g217963 BLASTN 1962 1e−170 96 Q1-K1-B12 216 3272 LIB3062-036- LIB3062 g217963 BLASTN 2115 1e−170 97 Q1-K1-F11 217 3272 LIB36-007- LIB36 g217963 BLASTN 1985 1e−169 95 Q1-E1-G2 218 3272 LIB3078-006- LIB3078 g217963 BLASTN 1876 1e−168 97 Q1-K1-C7 219 3272 LIB3078-034- LIB3078 g217963 BLASTN 1786 1e−165 98 Q1-K1-B7 220 3272 LIB36-009- LIB36 g217963 BLASTN 1921 1e−165 95 Q1-E1-H2 221 3272 LIB36-020- LIB36 g217963 BLASTN 1717 1e−164 92 Q1-E1-F10 222 3272 LIB3078-053- LIB3078 g217963 BLASTN 1874 1e−162 97 Q1-K1-D9 223 3272 LIB83-015- LIB83 g217963 BLASTN 1876 1e−161 91 Q1-E1-B8 224 3272 LIB36-004- LIB36 g217963 BLASTN 1429 1e−160 97 Q1-E1-D2 225 3272 LIB83-011- LIB83 g217963 BLASTN 1557 1e−160 95 Q1-E1-H7 226 3272 LIB3078-018- LIB3078 g217963 BLASTN 1844 1e−159 88 Q1-K1-H1 227 3272 LIB189-030- LIB189 g217963 BLASTN 1436 1e−152 97 Q1-E1-E9 228 3272 LIB189-006- LIB189 g217963 BLASTN 1825 1e−151 99 Q1-E1-F9 229 3272 LIB36-022- LIB36 g217963 BLASTN 1635 1e−150 97 Q1-E1-H3 230 3272 LIB83-011- LIB83 g217963 BLASTN 1414 1e−149 97 Q1-E1-D3 231 3272 LIB3062-047- LIB3062 g217963 BLASTN 1691 1e−148 89 Q1-K1-B2 232 3272 LIB36-016- LIB36 g217963 BLASTN 1719 1e−147 93 Q2-E2-D9 233 3272 LIB36-021- LIB36 g217963 BLASTN 1512 1e−144 93 Q1-E1-G3 234 3272 LIB3078-004- LIB3078 g217963 BLASTN 1787 1e−142 96 Q1-K1-B4 235 3272 LIB3068-056- LIB3068 g217963 BLASTN 1145 1e−141 91 Q1-K1-C6 236 3272 LIB3078-052- LIB3078 g217963 BLASTN 1340 1e−141 96 Q1-K1-F8 237 3272 LIB36-021- LIB36 g217963 BLASTN 1436 1e−139 93 Q1-E1-A6 238 3272 LIB189-028- LIB189 g217963 BLASTN 1617 1e−139 98 Q1-E1-B12 239 3272 LIB83-005- LIB83 g217963 BLASTN 1495 1e−133 92 Q1-E1-B3 240 3272 LIB3060-020- LIB3060 g217963 BLASTN 750 1e−132 88 Q1-K1-G10 241 3272 LIB36-013- LIB36 g217963 BLASTN 1367 1e−132 90 Q1-E1-E6 242 3272 LIB84-015- LIB84 g217963 BLASTN 1545 1e−132 92 Q1-E1-E1 243 3272 LIB36-006- LIB36 g217963 BLASTN 1640 1e−130 91 Q1-E1-E10 244 3272 LIB84-027- LIB84 g217963 BLASTN 1333 1e−128 95 Q1-E1-H12 245 3272 LIB3067-001- LIB3067 g217963 BLASTN 1364 1e−127 90 Q1-K1-B11 246 3272 LIB3062-016- LIB3062 g217963 BLASTN 1369 1e−127 89 Q1-K1-D11 247 3272 LIB3060-013- LIB3060 g217963 BLASTN 1607 1e−127 90 Q1-K1-D6 248 3272 LIB3078-028- LIB3078 g217963 BLASTN 906 1e−126 93 Q1-K1-F4 249 3272 LIB3067-027- LIB3067 g217963 BLASTN 1364 1e−125 92 Q1-K1-A8 250 3272 LIB189-034- LIB189 g217963 BLASTN 1139 1e−117 91 Q1-E1-B9 251 3272 LIB189-027- LIB189 g217963 BLASTN 1264 1e−116 85 Q1-E1-C2 252 3272 LIB3060-034- LIB3060 g217963 BLASTN 1490 1e−116 86 Q1-K1-E7 253 3272 LIB36-010- LIB36 g217963 BLASTN 1427 1e−115 88 Q1-E1-A10 254 3272 LIB3078-040- LIB3078 g217963 BLASTN 1475 1e−115 84 Q1-K1-E5 255 3272 LIB3078-052- LIB3078 g22464 BLASTN 1141 1e−113 92 Q1-K1-H4 256 3272 LIB3078-001- LIB3078 g217963 BLASTN 1173 1e−113 93 Q1-K1-B1 257 3272 LIB84-017- LIB84 g1673455 BLASTN 747 1e−112 91 Q1-E1-D1 258 3272 LIB3060-034- LIB3060 g217963 BLASTN 1135 1e−112 87 Q1-K1-B7 259 3272 LIB3060-028- LIB3060 g217963 BLASTN 1012 1e−111 88 Q1-K1-D3 260 3272 LIB36-017- LIB36 g217963 BLASTN 1398 1e−108 87 Q1-E1-B8 261 3272 LIB84-008- LIB84 g217963 BLASTN 964 1e−103 93 Q1-E1-G1 262 3272 LIB3078-027- LIB3078 g217963 BLASTN 894 1e−100 91 Q1-K1-D12 263 3272 LIB36-010- LIB36 g217963 BLASTN 1257 1e−100 92 Q1-E1-E7 264 3272 LIB3068-029- LIB3068 g217963 BLASTN 1044 1e−93 94 Q1-K1-F6 265 3272 LIB3060-014- LIB3060 g217963 BLASTN 934 1e−89 92 Q1-K1-D9 266 3272 LIB3060-023- LIB3060 g1673455 BLASTN 666 1e−88 96 Q1-K1-H3 267 3272 LIB84-023- LIB84 g1673455 BLASTN 947 1e−84 91 Q1-E1-B2 268 3272 LIB3062-015- LIB3062 g217963 BLASTN 1007 1e−75 95 Q1-K1-H5 269 3272 LIB36-013- LIB36 g1673455 BLASTN 976 1e−72 97 Q1-E1-H2 270 3272 LIB36-009- LIB36 g22464 BLASTN 881 1e−63 98 Q1-E1-F4 271 3272 46-LIB84- LIB84 g22464 BLASTN 449 1e−38 95 007-Q1-E1-D6 272 3272 LIB3078-054- LIB3078 g529673 BLASTN 349 1e−24 94 Q1-K1-D12 273 3272 LIB36-016- LIB36 g529673 BLASTN 342 1e−19 97 Q2-E2-D1 274 8171 LIB3066-019- LIB3066 g1673455 BLASTN 1193 1e−161 95 Q1-K1-H5 275 8171 LIB36-005- LIB36 g1673455 BLASTN 1260 1e−155 99 Q1-E1-C10 276 8171 LIB84-008- LIB84 g1673455 BLASTN 1300 1e−150 100 Q1-E1-E11 277 8171 LIB36-010- LIB36 g1673455 BLASTN 1484 1e−125 99 Q1-E1-B4 278 8171 LIB36-017- LIB36 g1673455 BLASTN 1206 1e−113 98 Q1-E1-D2 279 8171 LIB83-005- LIB83 g1673455 BLASTN 620 1e−85 93 Q1-E1-B2 280 8171 LIB36-022- LIB36 g1673455 BLASTN 729 1e−60 95 Q1-E1-E3 281 8171 LIB84-006- LIB84 g1673455 BLASTN 298 1e−15 67 Q1-E1-B2 SOYBEAN RIBULOSE-BISPHOSPHATE CARBOXYLASE 282 -700646133 700646133H1 SOYMON012 g1079735 BLASTN 249 1e−11 77 283 -700680902 700680902H1 SOYMON008 g1055367 BLASTN 454 1e−46 87 284 -700737728 700737728H1 SOYMON012 g1055367 BLASTN 241 1e−18 91 285 -700873832 700873832H1 SOYMON018 g1055367 BLASTN 424 1e−26 88 286 -700874452 700874452H1 SOYMON018 g1079735 BLASTN 209 1e−8 87 287 -700993404 700993404H1 SOYMON011 g1055367 BLASTN 508 1e−70 87 288 -700995052 700995052H1 SOYMON011 g1079735 BLASTN 235 1e−10 91 289 -701118676 701118676H1 SOYMON037 g1055367 BLASTN 427 1e−44 78 290 10981 700661710H1 SOYMON005 g3168587 BLASTX 194 1e−20 57 291 10981 700661109H1 SOYMON005 g3168587 BLASTX 128 1e−10 51 292 16 700680726H1 SOYMON008 g1055367 BLASTN 1262 1e−126 98 293 16 700680952H1 SOYMON008 g1055367 BLASTN 1362 1e−126 93 294 16 700680959H1 SOYMON008 g1055367 BLASTN 1151 1e−120 98 295 16 700763859H1 SOYMON018 g1055367 BLASTN 1472 1e−116 99 296 16 700557838H1 SOYMON001 g1055367 BLASTN 1456 1e−115 99 297 16 700558916H1 SOYMON001 g1055367 BLASTN 1441 1e−113 99 298 16 700680502H1 SOYMON008 g1055367 BLASTN 665 1e−112 96 299 16 700556877H1 SOYMON001 g1079735 BLASTN 743 1e−109 96 300 16 700606206H1 SOYMON008 g1055367 BLASTN 770 1e−109 100 301 16 700557609H1 SOYMON001 g1055367 BLASTN 1085 1e−109 99 302 16 700646293H1 SOYMON012 g1055367 BLASTN 1400 1e−109 100 303 16 700557441H1 SOYMON001 g1055367 BLASTN 1073 1e−108 99 304 16 700646203H1 SOYMON012 g1055367 BLASTN 1191 1e−108 98 305 16 700787408H2 SOYMON011 g1055367 BLASTN 1386 1e−108 99 306 16 700605320H2 SOYMON004 g1055367 BLASTN 1389 1e−108 99 307 16 700563581H1 SOYMON002 g1055367 BLASTN 1379 1e−107 98 308 16 700553939H1 SOYMON001 g1055367 BLASTN 1063 1e−106 99 309 16 701001329H1 SOYMON018 g1055367 BLASTN 1365 1e−106 97 310 16 700684042H1 SOYMON008 g1055367 BLASTN 1366 1e−106 99 311 16 700555971H1 SOYMON001 g1055367 BLASTN 708 1e−105 97 312 16 700654101H1 SOYMON003 g1055367 BLASTN 715 1e−105 98 313 16 700560889H1 SOYMON001 g1055367 BLASTN 716 1e−105 99 314 16 700963683H1 SOYMON022 g1055367 BLASTN 741 1e−105 98 315 16 700788007H1 SOYMON011 g1055367 BLASTN 1355 1e−105 100 316 16 700556641H1 SOYMON001 g1055367 BLASTN 1359 1e−105 99 317 16 700561084H1 SOYMON001 g1055367 BLASTN 1360 1e−105 100 318 16 700555936H1 SOYMON001 g1055367 BLASTN 720 1e−104 97 319 16 701059184H1 SOYMON033 g1055367 BLASTN 1192 1e−104 98 320 16 700739631H1 SOYMON012 g1055367 BLASTN 1346 1e−104 97 321 16 700683729H1 SOYMON008 g1055367 BLASTN 1346 1e−104 97 322 16 700555221H1 SOYMON001 g1055367 BLASTN 1351 1e−104 99 323 16 700680511H1 SOYMON008 g1079735 BLASTN 789 1e−103 95 324 16 700684247H1 SOYMON008 g1055367 BLASTN 1331 1e−103 99 325 16 700993018H1 SOYMON011 g1055367 BLASTN 1332 1e−103 98 326 16 700560424H1 SOYMON001 g1055367 BLASTN 1338 1e−103 95 327 16 700558552H1 SOYMON001 g1055367 BLASTN 630 1e−102 100 328 16 700980925H1 SOYMON009 g1055367 BLASTN 690 1e−102 98 329 16 700554035H1 SOYMON001 g1079735 BLASTN 730 1e−102 97 330 16 700787457H2 SOYMON011 g1055367 BLASTN 1005 1e−102 100 331 16 701066314H1 SOYMON034 g1055367 BLASTN 1115 1e−102 100 332 16 700984792H1 SOYMON009 g1055367 BLASTN 1327 1e−102 99 333 16 700993845H1 SOYMON011 g1055367 BLASTN 1256 1e−101 99 334 16 700553638H1 SOYMON001 g1055367 BLASTN 1281 1e−101 96 335 16 701108568H1 SOYMON036 g1055367 BLASTN 1309 1e−101 99 336 16 700730203H1 SOYMON009 g1055367 BLASTN 1309 1e−101 99 337 16 700686590H1 SOYMON008 g1055367 BLASTN 1310 1e−101 100 338 16 700684291H1 SOYMON008 g1055367 BLASTN 1313 1e−101 99 339 16 700686641H1 SOYMON008 g1055367 BLASTN 1317 1e−101 98 340 16 700739501H1 SOYMON012 g1055367 BLASTN 988 1e−100 99 341 16 700686672H1 SOYMON008 g1055367 BLASTN 989 1e−100 99 342 16 701105057H1 SOYMON036 g1055367 BLASTN 1170 1e−100 99 343 16 700560247H1 SOYMON001 g1055367 BLASTN 1259 1e−100 94 344 16 700685202H1 SOYMON008 g1055367 BLASTN 1269 1e−100 99 345 16 700741438H1 SOYMON012 g1055367 BLASTN 1296 1e−100 99 346 16 700987146H1 SOYMON009 g1055367 BLASTN 1298 1e−100 99 347 16 700874210H1 SOYMON018 g1055367 BLASTN 1298 1e−100 99 348 16 700558668H1 SOYMON001 g1055367 BLASTN 1299 1e−100 97 349 16 701066793H1 SOYMON034 g1055367 BLASTN 1299 1e−100 96 350 16 700897572H1 SOYMON027 g1055367 BLASTN 1301 1e−100 98 351 16 700788520H1 SOYMON011 g1055367 BLASTN 1304 1e−100 97 352 16 700993424H1 SOYMON011 g1055367 BLASTN 1306 1e−100 99 353 16 700990285H1 SOYMON011 g1055367 BLASTN 1307 1e−100 98 354 16 700559016H1 SOYMON001 g170057 BLASTN 703 1e−99 96 355 16 700684946H1 SOYMON008 g1055367 BLASTN 837 1e−99 96 356 16 700994454H1 SOYMON011 g1079735 BLASTN 891 1e−99 98 357 16 700684022H1 SOYMON008 g1055367 BLASTN 974 1e−99 99 358 16 700981572H1 SOYMON009 g1055367 BLASTN 977 1e−99 97 359 16 700547916H1 SOYMON001 g1055367 BLASTN 1018 1e−99 97 360 16 701210426H1 SOYMON035 g1055367 BLASTN 1175 1e−99 96 361 16 700680983H1 SOYMON008 g1055367 BLASTN 1178 1e−99 96 362 16 700686304H1 SOYMON008 g1055367 BLASTN 1213 1e−99 95 363 16 700656925H1 SOYMON004 g1055367 BLASTN 1248 1e−99 97 364 16 700959008H1 SOYMON022 g1055367 BLASTN 1286 1e−99 99 365 16 700990104H1 SOYMON011 g1055367 BLASTN 1286 1e−99 99 366 16 700733702H1 SOYMON010 g1055367 BLASTN 1291 1e−99 99 367 16 700679911H2 SOYMON008 g1055367 BLASTN 750 1e−98 100 368 16 700683580H1 SOYMON008 g1055367 BLASTN 975 1e−98 99 369 16 701000694H1 SOYMON018 g1055367 BLASTN 981 1e−98 98 370 16 700788434H1 SOYMON011 g1055367 BLASTN 993 1e−98 99 371 16 700977489H1 SOYMON009 g1055367 BLASTN 1115 1e−98 100 372 16 700646244H1 SOYMON012 g1055367 BLASTN 1245 1e−98 93 373 16 700789239H2 SOYMON011 g1055367 BLASTN 1275 1e−98 100 374 16 700941416H1 SOYMON024 g1055367 BLASTN 1277 1e−98 98 375 16 700741114H1 SOYMON012 g1055367 BLASTN 1280 1e−98 100 376 16 700787710H2 SOYMON011 g1055367 BLASTN 1280 1e−98 100 377 16 700738915H1 SOYMON012 g1055367 BLASTN 1281 1e−98 99 378 16 700681172H2 SOYMON008 g1055367 BLASTN 1281 1e−98 97 379 16 700989627H1 SOYMON011 g1055367 BLASTN 1283 1e−98 99 380 16 700992304H1 SOYMON011 g1055367 BLASTN 631 1e−97 95 381 16 700660092H1 SOYMON004 g1055367 BLASTN 655 1e−97 100 382 16 700742022H1 SOYMON012 g1079735 BLASTN 710 1e−97 98 383 16 700787646H2 SOYMON011 g1055367 BLASTN 755 1e−97 100 384 16 700686569H1 SOYMON008 g1055367 BLASTN 955 1e−97 99 385 16 701107113H1 SOYMON036 g1055367 BLASTN 959 1e−97 98 386 16 700553876H1 SOYMON001 g1055367 BLASTN 1186 1e−97 94 387 16 701106749H1 SOYMON036 g1055367 BLASTN 1194 1e−97 94 388 16 700660208H1 SOYMON004 g1055367 BLASTN 1219 1e−97 99 389 16 700738445H1 SOYMON012 g1055367 BLASTN 1263 1e−97 96 390 16 700873776H1 SOYMON018 g1055367 BLASTN 1265 1e−97 100 391 16 700684414H1 SOYMON008 g1055367 BLASTN 1265 1e−97 100 392 16 700790868H1 SOYMON011 g1055367 BLASTN 1268 1e−97 98 393 16 700787726H2 SOYMON011 g1055367 BLASTN 1270 1e−97 100 394 16 700899186H1 SOYMON027 g1055367 BLASTN 1271 1e−97 99 395 16 700726442H1 SOYMON009 g1055367 BLASTN 670 1e−96 100 396 16 700681422H2 SOYMON008 g1055367 BLASTN 680 1e−96 98 397 16 700901301H1 SOYMON027 g1055367 BLASTN 745 1e−96 100 398 16 701214546H1 SOYMON035 g1055367 BLASTN 943 1e−96 99 399 16 701211571H1 SOYMON035 g1055367 BLASTN 970 1e−96 100 400 16 701067621H1 SOYMON034 g1055367 BLASTN 1137 1e−96 92 401 16 700656975H1 SOYMON004 g1055367 BLASTN 1157 1e−96 99 402 16 700679981H2 SOYMON008 g1055367 BLASTN 1192 1e−96 98 403 16 700788456H1 SOYMON011 g1055367 BLASTN 1250 1e−96 98 404 16 700993650H1 SOYMON011 g1055367 BLASTN 1253 1e−96 98 405 16 700738760H1 SOYMON012 g1055367 BLASTN 1255 1e−96 100 406 16 700738920H1 SOYMON012 g1055367 BLASTN 1258 1e−96 99 407 16 700992293H1 SOYMON011 g1055367 BLASTN 1258 1e−96 98 408 16 700849079H1 SOYMON021 g1055367 BLASTN 1258 1e−96 97 409 16 700683157H1 SOYMON008 g1055367 BLASTN 1258 1e−96 99 410 16 700874075H1 SOYMON018 g1055367 BLASTN 1260 1e−96 100 411 16 700988186H1 SOYMON009 g1079735 BLASTN 638 1e−95 93 412 16 700899275H1 SOYMON027 g1055367 BLASTN 920 1e−95 99 413 16 700943511H1 SOYMON024 g1055367 BLASTN 930 1e−95 98 414 16 701062407H1 SOYMON033 g1055367 BLASTN 1026 1e−95 94 415 16 700991032H1 SOYMON011 g1055367 BLASTN 1070 1e−95 98 416 16 700740521H1 SOYMON012 g1055367 BLASTN 1187 1e−95 97 417 16 700685255H1 SOYMON008 g1055367 BLASTN 1191 1e−95 94 418 16 700846540H1 SOYMON021 g1055367 BLASTN 1203 1e−95 96 419 16 700684186H1 SOYMON008 g1055367 BLASTN 1239 1e−95 99 420 16 700565092H1 SOYMON002 g1055367 BLASTN 1239 1e−95 97 421 16 700898668H1 SOYMON027 g1055367 BLASTN 1240 1e−95 100 422 16 700997221H1 SOYMON018 g1055367 BLASTN 1240 1e−95 100 423 16 700737823H1 SOYMON012 g1055367 BLASTN 1240 1e−95 100 424 16 700740566H1 SOYMON012 g1055367 BLASTN 1241 1e−95 99 425 16 700726057H1 SOYMON009 g1055367 BLASTN 1241 1e−95 99 426 16 700658843H1 SOYMON004 g1055367 BLASTN 1243 1e−95 99 427 16 700737902H1 SOYMON012 g1055367 BLASTN 1244 1e−95 97 428 16 700873809H1 SOYMON018 g1055367 BLASTN 1246 1e−95 99 429 16 701210184H1 SOYMON035 g1055367 BLASTN 508 1e−94 96 430 16 700874925H1 SOYMON018 g1055367 BLASTN 655 1e−94 98 431 16 700686258H1 SOYMON008 g1055367 BLASTN 657 1e−94 98 432 16 700742042H1 SOYMON012 g1055367 BLASTN 659 1e−94 97 433 16 700679995H2 SOYMON008 g1055367 BLASTN 731 1e−94 96 434 16 700682014H1 SOYMON008 g1079735 BLASTN 800 1e−94 96 435 16 700741910H1 SOYMON012 g1055367 BLASTN 906 1e−94 98 436 16 701107208H1 SOYMON036 g1055367 BLASTN 907 1e−94 98 437 16 700896405H1 SOYMON027 g1055367 BLASTN 936 1e−94 99 438 16 700961649H1 SOYMON022 g1055367 BLASTN 941 1e−94 96 439 16 700555260H1 SOYMON001 g1055367 BLASTN 1141 1e−94 97 440 16 700646292H1 SOYMON012 g1055367 BLASTN 1155 1e−94 93 441 16 700896794H1 SOYMON027 g1055367 BLASTN 1164 1e−94 99 442 16 700900448H1 SOYMON027 g1055367 BLASTN 1227 1e−94 95 443 16 700978796H1 SOYMON009 g1055367 BLASTN 1228 1e−94 99 444 16 700874579H1 SOYMON018 g1055367 BLASTN 1229 1e−94 99 445 16 700989693H1 SOYMON011 g1055367 BLASTN 1229 1e−94 99 446 16 700872477H1 SOYMON018 g1055367 BLASTN 1230 1e−94 98 447 16 700873947H1 SOYMON018 g1055367 BLASTN 1233 1e−94 99 448 16 700740463H1 SOYMON012 g1055367 BLASTN 1234 1e−94 99 449 16 700846439H1 SOYMON021 g1055367 BLASTN 1235 1e−94 100 450 16 701143505H2 SOYMON038 g1055367 BLASTN 1235 1e−94 100 451 16 700876930H1 SOYMON018 g1055367 BLASTN 1237 1e−94 98 452 16 700787131H2 SOYMON011 g1055367 BLASTN 480 1e−93 98 453 16 701107174H1 SOYMON036 g1055367 BLASTN 908 1e−93 99 454 16 700683318H1 SOYMON008 g1055367 BLASTN 921 1e−93 97 455 16 700738122H1 SOYMON012 g1055367 BLASTN 935 1e−93 100 456 16 700683238H1 SOYMON008 g1055367 BLASTN 975 1e−93 99 457 16 700741164H1 SOYMON012 g1055367 BLASTN 1014 1e−93 98 458 16 700896476H1 SOYMON027 g1055367 BLASTN 1075 1e−93 100 459 16 700993971H1 SOYMON011 g1055367 BLASTN 1149 1e−93 94 460 16 700895401H1 SOYMON027 g1055367 BLASTN 1171 1e−93 99 461 16 700790223H2 SOYMON011 g1055367 BLASTN 1215 1e−93 98 462 16 700945189H1 SOYMON024 g1055367 BLASTN 1215 1e−93 100 463 16 700741390H1 SOYMON012 g1055367 BLASTN 1215 1e−93 100 464 16 700737811H1 SOYMON012 g1055367 BLASTN 1219 1e−93 99 465 16 700785969H2 SOYMON011 g1055367 BLASTN 1220 1e−93 100 466 16 700740478H1 SOYMON012 g1055367 BLASTN 1220 1e−93 100 467 16 700790742H1 SOYMON011 g1055367 BLASTN 1221 1e−93 99 468 16 700740462H1 SOYMON012 g1055367 BLASTN 1222 1e−93 98 469 16 700657760H1 SOYMON004 g1055367 BLASTN 1224 1e−93 99 470 16 700659336H1 SOYMON004 g1055367 BLASTN 1225 1e−93 96 471 16 700790904H1 SOYMON011 g1055367 BLASTN 616 1e−92 99 472 16 700738911H1 SOYMON012 g1055367 BLASTN 741 1e−92 100 473 16 700872532H1 SOYMON018 g1055367 BLASTN 743 1e−92 99 474 16 700967765H1 SOYMON033 g1055367 BLASTN 896 1e−92 99 475 16 700876909H1 SOYMON018 g1055367 BLASTN 913 1e−92 98 476 16 700989032H1 SOYMON011 g1055367 BLASTN 971 1e−92 99 477 16 700872401H1 SOYMON018 g1055367 BLASTN 1011 1e−92 98 478 16 701104761H1 SOYMON036 g1055367 BLASTN 1133 1e−92 93 479 16 700787439H2 SOYMON011 g1055367 BLASTN 1133 1e−92 93 480 16 700682703H1 SOYMON008 g1055367 BLASTN 1136 1e−92 93 481 16 700788179H1 SOYMON011 g1055367 BLASTN 1155 1e−92 98 482 16 700724905H1 SOYMON009 g1055367 BLASTN 1173 1e−92 98 483 16 700660182H1 SOYMON004 g1055367 BLASTN 1208 1e−92 99 484 16 700876415H1 SOYMON018 g1055367 BLASTN 1208 1e−92 99 485 16 700738544H1 SOYMON012 g1055367 BLASTN 1210 1e−92 100 486 16 700894558H1 SOYMON024 g1055367 BLASTN 1211 1e−92 99 487 16 700740901H1 SOYMON012 g1055367 BLASTN 428 1e−91 97 488 16 700683039H1 SOYMON008 g1055367 BLASTN 621 1e−91 97 489 16 700980945H1 SOYMON009 g1055367 BLASTN 624 1e−91 93 490 16 700557890H1 SOYMON001 g1055367 BLASTN 871 1e−91 97 491 16 700863566H1 SOYMON027 g1055367 BLASTN 1127 1e−91 95 492 16 701108362H1 SOYMON036 g1055367 BLASTN 1129 1e−91 95 493 16 700658190H1 SOYMON004 g1055367 BLASTN 1136 1e−91 94 494 16 700994486H1 SOYMON011 g1055367 BLASTN 1144 1e−91 94 495 16 700553851H1 SOYMON001 g1055367 BLASTN 1151 1e−91 93 496 16 700683005H1 SOYMON008 g1055367 BLASTN 1159 1e−91 98 497 16 700789709H1 SOYMON011 g1055367 BLASTN 1191 1e−91 99 498 16 700752960H1 SOYMON014 g1055367 BLASTN 1196 1e−91 99 499 16 700959845H1 SOYMON022 g1055367 BLASTN 1196 1e−91 99 500 16 700738866H1 SOYMON012 g1055367 BLASTN 1201 1e−91 99 501 16 701064223H1 SOYMON034 g1055367 BLASTN 510 1e−90 98 502 16 701002414H1 SOYMON018 g1055367 BLASTN 577 1e−90 97 503 16 700992711H1 SOYMON011 g1055367 BLASTN 751 1e−90 98 504 16 700680079H2 SOYMON008 g1055367 BLASTN 807 1e−90 97 505 16 700992131H1 SOYMON011 g1055367 BLASTN 814 1e−90 98 506 16 700945939H1 SOYMON024 g1055367 BLASTN 872 1e−90 98 507 16 700995283H1 SOYMON011 g1055367 BLASTN 896 1e−90 97 508 16 700790720H1 SOYMON011 g1055367 BLASTN 898 1e−90 98 509 16 700557607H1 SOYMON001 g1055367 BLASTN 908 1e−90 91 510 16 701146551H1 SOYMON031 g1055367 BLASTN 923 1e−90 98 511 16 701002369H1 SOYMON018 g1055367 BLASTN 953 1e−90 99 512 16 700682563H2 SOYMON008 g1055367 BLASTN 1045 1e−90 100 513 16 700555211H1 SOYMON001 g1055367 BLASTN 1115 1e−90 100 514 16 700656287H1 SOYMON004 g1055367 BLASTN 1117 1e−90 96 515 16 700791902H1 SOYMON011 g1055367 BLASTN 1182 1e−90 98 516 16 700876346H1 SOYMON018 g1055367 BLASTN 1183 1e−90 96 517 16 700681759H1 SOYMON008 g1055367 BLASTN 1183 1e−90 99 518 16 701105254H1 SOYMON036 g1055367 BLASTN 1185 1e−90 100 519 16 700873322H1 SOYMON018 g1055367 BLASTN 1187 1e−90 98 520 16 700741118H1 SOYMON012 g1055367 BLASTN 1188 1e−90 96 521 16 700681782H1 SOYMON008 g1055367 BLASTN 1190 1e−90 100 522 16 700746782H1 SOYMON013 g1055367 BLASTN 1190 1e−90 100 523 16 700656875H1 SOYMON004 g1079735 BLASTN 736 1e−89 97 524 16 700993783H1 SOYMON011 g1055367 BLASTN 800 1e−89 100 525 16 700738524H1 SOYMON012 g1055367 BLASTN 846 1e−89 98 526 16 701214655H1 SOYMON035 g1055367 BLASTN 881 1e−89 98 527 16 700740449H1 SOYMON012 g1055367 BLASTN 924 1e−89 97 528 16 700556379H1 SOYMON001 g1055367 BLASTN 1096 1e−89 95 529 16 700660523H1 SOYMON004 g1055367 BLASTN 1097 1e−89 92 530 16 700791055H1 SOYMON011 g1055367 BLASTN 1173 1e−89 99 531 16 700656671H1 SOYMON004 g1055367 BLASTN 1175 1e−89 93 532 16 700740963H1 SOYMON012 g1055367 BLASTN 616 1e−88 99 533 16 701107017H1 SOYMON036 g1055367 BLASTN 617 1e−88 96 534 16 701139539H1 SOYMON038 g1055367 BLASTN 644 1e−88 95 535 16 700946365H1 SOYMON024 g170057 BLASTN 649 1e−88 97 536 16 700682509H2 SOYMON008 g1055367 BLASTN 844 1e−88 97 537 16 700994024H1 SOYMON011 g1055367 BLASTN 844 1e−88 98 538 16 700659886H1 SOYMON004 g1055367 BLASTN 850 1e−88 98 539 16 700755378H1 SOYMON014 g1055367 BLASTN 881 1e−88 98 540 16 700847182H1 SOYMON021 g1055367 BLASTN 916 1e−88 97 541 16 700789017H2 SOYMON011 g1055367 BLASTN 1110 1e−88 96 542 16 700657694H1 SOYMON004 g1055367 BLASTN 1160 1e−88 97 543 16 700894533H1 SOYMON024 g1055367 BLASTN 1164 1e−88 99 544 16 700989594H1 SOYMON011 g1055367 BLASTN 1166 1e−88 99 545 16 700560570H1 SOYMON001 g1055367 BLASTN 978 1e−87 97 546 16 700656095H1 SOYMON004 g1055367 BLASTN 1056 1e−87 95 547 16 700656137H1 SOYMON004 g1055367 BLASTN 1100 1e−87 100 548 16 700900212H1 SOYMON027 g1055367 BLASTN 1106 1e−87 98 549 16 700871945H1 SOYMON018 g1055367 BLASTN 1150 1e−87 100 550 16 701144650H1 SOYMON031 g1055367 BLASTN 1154 1e−87 99 551 16 700740357H1 SOYMON012 g1055367 BLASTN 566 1e−86 100 552 16 700790635H2 SOYMON011 g1079735 BLASTN 630 1e−86 98 553 16 700843795H1 SOYMON021 g1055367 BLASTN 834 1e−86 97 554 16 700790207H2 SOYMON011 g1055367 BLASTN 1062 1e−86 94 555 16 700725303H1 SOYMON009 g1055367 BLASTN 1064 1e−86 94 556 16 700739809H1 SOYMON012 g1055367 BLASTN 1067 1e−86 94 557 16 700659535H1 SOYMON004 g1055367 BLASTN 1068 1e−86 92 558 16 700740653H1 SOYMON012 g1055367 BLASTN 1071 1e−86 94 559 16 700993558H1 SOYMON011 g1055367 BLASTN 1071 1e−86 94 560 16 701153296H1 SOYMON031 g1079735 BLASTN 1101 1e−86 99 561 16 700992113H1 SOYMON011 g1055367 BLASTN 1104 1e−86 98 562 16 700555503H1 SOYMON001 g1055367 BLASTN 1133 1e−86 89 563 16 700792226H1 SOYMON011 g170057 BLASTN 1142 1e−86 99 564 16 701105302H1 SOYMON036 g1055367 BLASTN 1143 1e−86 89 565 16 700871129H1 SOYMON018 g1055367 BLASTN 1143 1e−86 94 566 16 700654859H1 SOYMON004 g1055367 BLASTN 519 1e−85 97 567 16 700656039H1 SOYMON004 g1055367 BLASTN 615 1e−85 98 568 16 700739061H1 SOYMON012 g1055367 BLASTN 642 1e−85 96 569 16 700655048H1 SOYMON004 g1055367 BLASTN 689 1e−85 95 570 16 700680540H1 SOYMON008 g1055367 BLASTN 696 1e−85 98 571 16 700730791H1 SOYMON009 g1055367 BLASTN 811 1e−85 99 572 16 700991246H1 SOYMON011 g1055367 BLASTN 893 1e−85 95 573 16 700876824H1 SOYMON018 g1055367 BLASTN 967 1e−85 98 574 16 700791594H1 SOYMON011 g1055367 BLASTN 1054 1e−85 94 575 16 700739144H1 SOYMON012 g1055367 BLASTN 1090 1e−85 100 576 16 700872171H1 SOYMON018 g1055367 BLASTN 1121 1e−85 99 577 16 700871089H1 SOYMON018 g1055367 BLASTN 1122 1e−85 95 578 16 700787735H2 SOYMON011 g1055367 BLASTN 1123 1e−85 95 579 16 700791676H1 SOYMON011 g1055367 BLASTN 1124 1e−85 96 580 16 700737752H1 SOYMON012 g1055367 BLASTN 1128 1e−85 92 581 16 700681539H1 SOYMON008 g1055367 BLASTN 495 1e−84 97 582 16 700994222H1 SOYMON011 g1055367 BLASTN 653 1e−84 99 583 16 701000001H1 SOYMON018 g1055367 BLASTN 743 1e−84 97 584 16 700874142H1 SOYMON018 g1055367 BLASTN 803 1e−84 99 585 16 701106980H1 SOYMON036 g1055367 BLASTN 837 1e−84 98 586 16 700684527H1 SOYMON008 g1055367 BLASTN 959 1e−84 98 587 16 700738477H1 SOYMON012 g1055367 BLASTN 1111 1e−84 99 588 16 701155411H1 SOYMON031 g1055367 BLASTN 1112 1e−84 99 589 16 700994428H1 SOYMON011 g170057 BLASTN 457 1e−83 98 590 16 700738079H1 SOYMON012 g1079735 BLASTN 496 1e−83 95 591 16 700658259H1 SOYMON004 g1055367 BLASTN 510 1e−83 98 592 16 701062095H1 SOYMON033 g1055367 BLASTN 599 1e−83 94 593 16 700730588H1 SOYMON009 g1055367 BLASTN 652 1e−83 95 594 16 700900426H1 SOYMON027 g1055367 BLASTN 653 1e−83 96 595 16 700994405H1 SOYMON011 g1055367 BLASTN 760 1e−83 98 596 16 700743222H1 SOYMON012 g1055367 BLASTN 874 1e−83 98 597 16 701108454H1 SOYMON036 g1055367 BLASTN 908 1e−83 91 598 16 701061556H1 SOYMON033 g1055367 BLASTN 936 1e−83 99 599 16 700871533H1 SOYMON018 g1055367 BLASTN 1097 1e−83 99 600 16 700558546H1 SOYMON001 g1079735 BLASTN 408 1e−82 95 601 16 700741006H1 SOYMON012 g1055367 BLASTN 446 1e−82 95 602 16 700994239H1 SOYMON011 g1055367 BLASTN 611 1e−82 94 603 16 700685501H1 SOYMON008 g1055367 BLASTN 620 1e−82 100 604 16 700741993H1 SOYMON012 g1055367 BLASTN 775 1e−82 100 605 16 700741994H1 SOYMON012 g1055367 BLASTN 780 1e−82 100 606 16 700741275H1 SOYMON012 g1055367 BLASTN 955 1e−82 100 607 16 700741979H1 SOYMON012 g1055367 BLASTN 1038 1e−82 95 608 16 700873834H1 SOYMON018 g1055367 BLASTN 1088 1e−82 98 609 16 700872831H1 SOYMON018 g1055367 BLASTN 710 1e−81 96 610 16 700684862H1 SOYMON008 g1055367 BLASTN 772 1e−81 98 611 16 700991906H1 SOYMON011 g1055367 BLASTN 777 1e−81 98 612 16 700655544H1 SOYMON004 g1055367 BLASTN 840 1e−81 98 613 16 700740768H1 SOYMON012 g1055367 BLASTN 1007 1e−81 99 614 16 700992972H1 SOYMON011 g1055367 BLASTN 1073 1e−81 97 615 16 700740745H1 SOYMON012 g1055367 BLASTN 1079 1e−81 99 616 16 700728041H1 SOYMON009 g1055367 BLASTN 1080 1e−81 87 617 16 700729690H1 SOYMON009 g1055367 BLASTN 1083 1e−81 95 618 16 700743048H1 SOYMON012 g1055367 BLASTN 388 1e−80 92 619 16 700790361H2 SOYMON011 g1055367 BLASTN 588 1e−80 93 620 16 700896585H1 SOYMON027 g1055367 BLASTN 588 1e−80 100 621 16 701104185H1 SOYMON036 g1055367 BLASTN 740 1e−80 99 622 16 700741286H1 SOYMON012 g1055367 BLASTN 756 1e−80 99 623 16 700737954H1 SOYMON012 g1055367 BLASTN 916 1e−80 91 624 16 700738883H1 SOYMON012 g1055367 BLASTN 1070 1e−80 94 625 16 700872433H1 SOYMON018 g170057 BLASTN 416 1e−79 94 626 16 701059827H1 SOYMON033 g1055367 BLASTN 438 1e−79 95 627 16 701117550H2 SOYMON037 g1055367 BLASTN 488 1e−79 96 628 16 700743227H1 SOYMON012 g1055367 BLASTN 670 1e−79 96 629 16 700990060H1 SOYMON011 g1079735 BLASTN 688 1e−79 96 630 16 700789891H2 SOYMON011 g1079735 BLASTN 892 1e−79 98 631 16 700739160H1 SOYMON012 g1055367 BLASTN 1008 1e−79 95 632 16 700900244H1 SOYMON027 g1055367 BLASTN 1051 1e−79 85 633 16 700680230H2 SOYMON008 g1055367 BLASTN 1057 1e−79 93 634 16 700991489H1 SOYMON011 g1055367 BLASTN 520 1e−78 94 635 16 700744694H1 SOYMON013 g1055367 BLASTN 521 1e−78 97 636 16 700659755H1 SOYMON004 g1055367 BLASTN 711 1e−78 92 637 16 700741013H1 SOYMON012 g1055367 BLASTN 730 1e−78 91 638 16 700990946H1 SOYMON011 g1079735 BLASTN 1046 1e−78 99 639 16 700791542H1 SOYMON011 g1055367 BLASTN 625 1e−77 97 640 16 700682942H1 SOYMON008 g1055367 BLASTN 683 1e−77 98 641 16 700994722H1 SOYMON011 g1055367 BLASTN 801 1e−77 93 642 16 700788601H1 SOYMON011 g1055367 BLASTN 1036 1e−77 99 643 16 700872290H1 SOYMON018 g1079735 BLASTN 1040 1e−77 98 644 16 700741012H1 SOYMON012 g1055367 BLASTN 386 1e−76 95 645 16 700990993H1 SOYMON011 g1055367 BLASTN 712 1e−76 96 646 16 700870628H1 SOYMON018 g1055367 BLASTN 760 1e−76 95 647 16 700740220H1 SOYMON012 g1055367 BLASTN 830 1e−76 94 648 16 700683853H1 SOYMON008 g1079735 BLASTN 972 1e−76 98 649 16 700657177H1 SOYMON004 g1055367 BLASTN 986 1e−76 99 650 16 700740956H1 SOYMON012 g1055367 BLASTN 553 1e−75 93 651 16 700683812H1 SOYMON008 g1055367 BLASTN 672 1e−75 98 652 16 701058565H1 SOYMON033 g1055367 BLASTN 834 1e−75 96 653 16 700789725H1 SOYMON011 g1079735 BLASTN 1014 1e−75 98 654 16 700787907H1 SOYMON011 g1055367 BLASTN 546 1e−74 92 655 16 700870534H1 SOYMON018 g170057 BLASTN 646 1e−74 92 656 16 700743023H1 SOYMON012 g1055367 BLASTN 656 1e−74 93 657 16 700557205H1 SOYMON001 g1079735 BLASTN 775 1e−74 93 658 16 700646080H1 SOYMON011 g1055367 BLASTN 926 1e−74 97 659 16 700998541H1 SOYMON018 g1055367 BLASTN 703 1e−73 100 660 16 700684330H1 SOYMON008 g1079735 BLASTN 863 1e−73 94 661 16 700739656H1 SOYMON012 g1055367 BLASTN 987 1e−73 88 662 16 700739768H1 SOYMON012 g1055367 BLASTN 481 1e−72 88 663 16 700683980H1 SOYMON008 g1055367 BLASTN 654 1e−72 92 664 16 700743962H1 SOYMON012 g1079735 BLASTN 975 1e−72 100 665 16 700742888H1 SOYMON012 g1079735 BLASTN 960 1e−71 100 666 16 700744006H1 SOYMON012 g1079735 BLASTN 962 1e−71 97 667 16 700871648H1 SOYMON018 g1055367 BLASTN 887 1e−70 92 668 16 700656924H1 SOYMON004 g1055367 BLASTN 361 1e−69 88 669 16 700743814H1 SOYMON012 g1079735 BLASTN 942 1e−69 98 670 16 700995036H1 SOYMON011 g1079735 BLASTN 930 1e−68 97 671 16 700991405H1 SOYMON011 g1079735 BLASTN 477 1e−67 96 672 16 700741463H1 SOYMON012 g1055367 BLASTN 537 1e−67 87 673 16 700870507H1 SOYMON018 g1055367 BLASTN 566 1e−67 94 674 16 701123032H1 SOYMON037 g1055367 BLASTN 687 1e−67 85 675 16 700946185H1 SOYMON024 g1055367 BLASTN 862 1e−67 96 676 16 700994265H1 SOYMON011 g1055367 BLASTN 907 1e−67 86 677 16 700742553H1 SOYMON012 g1055367 BLASTN 626 1e−66 98 678 16 700655130H1 SOYMON004 g1055367 BLASTN 895 1e−66 80 679 16 700656978H1 SOYMON004 g1055367 BLASTN 905 1e−66 82 680 16 700743939H1 SOYMON012 g1055367 BLASTN 570 1e−65 100 681 16 700742580H1 SOYMON012 g1055367 BLASTN 580 1e−65 99 682 16 700872884H1 SOYMON018 g1079735 BLASTN 737 1e−65 92 683 16 701157394H1 SOYMON031 g1079735 BLASTN 479 1e−64 95 684 16 700992046H1 SOYMON011 g1079735 BLASTN 853 1e−62 99 685 16 700808471H1 SOYMON024 g18755 BLASTN 805 1e−60 100 686 16 700992056H1 SOYMON011 g1055367 BLASTN 830 1e−60 100 687 16 700975486H1 SOYMON009 g1055367 BLASTN 764 1e−59 93 688 16 700894434H1 SOYMON024 g1055367 BLASTN 622 1e−58 95 689 16 700992089H1 SOYMON011 g1055367 BLASTN 805 1e−58 100 690 16 700744590H1 SOYMON013 g1055367 BLASTN 541 1e−56 90 691 16 700787253H2 SOYMON011 g1055367 BLASTN 783 1e−56 95 692 16 700726279H1 SOYMON009 g1055367 BLASTN 604 1e−55 97 693 16 700995242H1 SOYMON011 g1079735 BLASTN 662 1e−55 82 694 16 700659992H1 SOYMON004 g1055367 BLASTN 768 1e−55 98 695 16 700994961H1 SOYMON011 g1055367 BLASTN 756 1e−54 96 696 16 700742875H1 SOYMON012 g1055367 BLASTN 758 1e−54 93 697 16 700995941H1 SOYMON018 g1055367 BLASTN 436 1e−52 98 698 16 700743887H1 SOYMON012 g1055367 BLASTN 446 1e−51 99 699 16 700656790H1 SOYMON004 g1055367 BLASTN 484 1e−50 89 700 16 700902134H1 SOYMON027 g1055367 BLASTN 711 1e−50 99 701 16 700996857H1 SOYMON018 g1079735 BLASTN 715 1e−50 100 702 16 700685138H1 SOYMON008 g1055367 BLASTN 385 1e−49 97 703 16 700738218H1 SOYMON012 g1079735 BLASTN 701 1e−49 99 704 16 700740869H1 SOYMON012 g1055367 BLASTN 680 1e−48 100 705 16 701002564H1 SOYMON018 g1079735 BLASTN 688 1e−48 99 706 16 700900791H1 SOYMON027 g1055367 BLASTN 361 1e−46 97 707 16 701109964H1 SOYMON036 g1055367 BLASTN 441 1e−45 87 708 16 700991810H1 SOYMON011 g1055367 BLASTN 377 1e−44 92 709 16 700786845H2 SOYMON011 g170057 BLASTN 440 1e−42 95 710 16 700655630H1 SOYMON004 g1055367 BLASTN 486 1e−42 97 711 16 700739315H1 SOYMON012 g1079735 BLASTN 610 1e−42 100 712 16 700788023H1 SOYMON011 g1055367 BLASTN 602 1e−41 75 713 16 700743017H1 SOYMON012 g170057 BLASTN 349 1e−40 89 714 16 700739471H1 SOYMON012 g1055367 BLASTN 590 1e−40 100 715 16 700740508H1 SOYMON012 g1079735 BLASTN 593 1e−40 99 716 16 700790942H1 SOYMON011 g170057 BLASTN 597 1e−40 86 717 16 700902452H1 SOYMON027 g1079735 BLASTN 395 1e−39 96 718 16 700658005H1 SOYMON004 g1079735 BLASTN 575 1e−39 100 719 16 700739396H1 SOYMON012 g1079735 BLASTN 565 1e−38 100 720 16 700863675H1 SOYMON027 g1055367 BLASTN 346 1e−37 93 721 16 700657081H1 SOYMON004 g1055367 BLASTN 461 1e−37 89 722 16 700743310H1 SOYMON012 g1055367 BLASTN 557 1e−37 96 723 16 700739139H1 SOYMON012 g1079735 BLASTN 543 1e−36 99 724 16 700742781H1 SOYMON012 g1055367 BLASTN 355 1e−35 100 725 16 700742729H1 SOYMON012 g1079735 BLASTN 532 1e−35 96 726 16 700740842H1 SOYMON012 g1055367 BLASTN 204 1e−32 97 727 16 700730732H1 SOYMON009 g1055367 BLASTN 320 1e−32 94 728 16 700742728H1 SOYMON012 g1055367 BLASTN 482 1e−31 94 729 16 700845311H1 SOYMON021 g1055367 BLASTN 483 1e−31 98 730 16 700874150H1 SOYMON018 g18754 BLASTN 340 1e−30 93 731 16 700958782H1 SOYMON022 g1055367 BLASTN 475 1e−30 100 732 16 700729671H1 SOYMON009 g1079735 BLASTN 310 1e−26 97 733 16 700989477H1 SOYMON011 g1055367 BLASTN 358 1e−26 98 734 16 700790532H2 SOYMON011 g1055367 BLASTN 330 1e−24 99 735 16 700895830H1 SOYMON027 g1055367 BLASTN 286 1e−23 96 736 16 700560643H1 SOYMON001 g1055367 BLASTN 295 1e−21 92 737 16 700559990H1 SOYMON001 g1079735 BLASTN 238 1e−20 98 738 16 700895956H1 SOYMON027 g1055367 BLASTN 193 1e−19 97 739 16 700680886H1 SOYMON008 g1055367 BLASTN 230 1e−17 82 740 16 700738267H1 SOYMON012 g1055367 BLASTN 246 1e−15 99 741 16 700741928H1 SOYMON012 g1055367 BLASTN 207 1e−12 90 742 16 700657321H1 SOYMON004 g1536889 BLASTX 92 1e−11 88 743 16 700742542H1 SOYMON012 g1079735 BLASTN 212 1e−10 97 744 16 700789463H2 SOYMON011 g1055367 BLASTN 159 1e−8 89 745 317 700998406H1 SOYMON018 g2323417 BLASTN 258 1e−33 80 746 317 700733345H1 SOYMON010 g2323461 BLASTN 292 1e−33 85 747 317 700681456H2 SOYMON008 g2323417 BLASTN 239 1e−23 79 748 317 700992806H1 SOYMON011 g2323461 BLASTN 252 1e−12 62 749 -GM16862 LIB3055-001- LIB3055 g1055367 BLASTN 482 1e−71 89 Q1-B1-G3 750 -GM16898 LIB3055-001- LIB3055 g1055367 BLASTN 594 1e−59 97 Q1-B1-H4 751 -GM17216 LIB3055-012- LIB3055 g1055367 BLASTN 299 1e−44 90 Q1-N1-H2 752 -GM30860 LIB3050-005- LIB3050 g21049 BLASTN 262 1e−21 68 Q1-K1-D5 753 -GM45237 LIB3073-001- LIB3073 g1055367 BLASTN 570 1e−38 64 Q1-K1-F7 754 -GM45275 LIB3073-001- LIB3073 g170057 BLASTN 665 1e−90 83 Q1-K1-H6 755 -GM45440 LIB3073-023- LIB3073 g1055367 BLASTN 906 1e−66 76 Q1-K1-A11 756 16 LIB3055-005- LIB3055 g1055367 BLASTN 1704 1e−166 98 Q1-N1-D8 757 16 LIB3073-023- LIB3073 g1055367 BLASTN 2074 1e−166 98 Q1-K1-C6 758 16 LIB3073-013- LIB3073 g1055367 BLASTN 2057 1e−165 99 Q1-K1-A5 759 16 LIB3055-007- LIB3055 g1055367 BLASTN 2065 1e−165 99 Q1-N1-E4 760 16 LIB3055-009- LIB3055 g1055367 BLASTN 2067 1e−165 98 Q1-N1-A9 761 16 LIB3055-008- LIB3055 g1055367 BLASTN 2047 1e−164 99 Q1-N1-C9 762 16 LIB3030-009- LIB3030 g1055367 BLASTN 823 1e−163 96 Q1-B1-G2 763 16 LIB3040-002- LIB3040 g1055367 BLASTN 1623 1e−163 97 Q1-E1-A4 764 16 LIB3073-023- LIB3073 g1055367 BLASTN 1671 1e−163 96 Q1-K1-E8 765 16 LIB3073-006- LIB3073 g1055367 BLASTN 2040 1e−163 100 Q1-K1-E8 766 16 LIB3053-010- LIB3053 g1055367 BLASTN 2023 1e−162 99 Q1-N1-E7 767 16 LIB3073-024- LIB3073 g1055367 BLASTN 1608 1e−161 99 Q1-K1-H4 768 16 LIB3055-008- LIB3055 g1055367 BLASTN 2008 1e−161 97 Q1-N1-A7 769 16 LIB3073-001- LIB3073 g1055367 BLASTN 1078 1e−160 98 Q1-K1-B10 770 16 LIB3055-013- LIB3055 g1055367 BLASTN 1726 1e−160 96 Q1-N1-B2 771 16 LIB3073-002- LIB3073 g1055367 BLASTN 1728 1e−160 96 Q1-K1-C1 772 16 LIB3073-013- LIB3073 g1055367 BLASTN 1904 1e−160 99 Q1-K1-F11 773 16 LIB3073-022- LIB3073 g1055367 BLASTN 1885 1e−159 100 Q1-K1-A11 774 16 LIB3073-026- LIB3073 g1055367 BLASTN 1987 1e−159 99 Q1-K1-G9 775 16 LIB3073-026- LIB3073 g1055367 BLASTN 1991 1e−159 99 Q1-K1-F9 776 16 LIB3073-024- LIB3073 g1055367 BLASTN 1740 1e−158 99 Q1-K1-A10 777 16 LIB3073-012- LIB3073 g1055367 BLASTN 1876 1e−158 98 Q1-K1-D7 778 16 LIB3049-013- LIB3049 g1055367 BLASTN 1265 1e−157 99 Q1-E1-B3 779 16 LIB3053-014- LIB3053 g1055367 BLASTN 1592 1e−157 97 Q1-N1-F9 780 16 LIB3054-003- LIB3054 g1055367 BLASTN 1949 1e−156 99 Q1-N1-G12 781 16 LIB3053-001- LIB3053 g1055367 BLASTN 1935 1e−155 100 Q1-B1-B3 782 16 LIB3027-005- LIB3027 g1055367 BLASTN 1943 1e−155 99 Q1-B1-F12 783 16 LIB3054-001- LIB3054 g1055367 BLASTN 1945 1e−155 100 Q1-B1-E6 784 16 LIB3055-007- LIB3055 g1055367 BLASTN 1691 1e−154 95 Q1-N1-G11 785 16 LIB3073-026- LIB3073 g1055367 BLASTN 1917 1e−153 99 Q1-K1-D12 786 16 LIB3053-009- LIB3053 g1055367 BLASTN 1919 1e−153 98 Q1-N1-C6 787 16 LIB3073-013- LIB3073 g1055367 BLASTN 1740 1e−151 98 Q1-K1-C1 788 16 LIB3073-006- LIB3073 g1055367 BLASTN 1789 1e−151 95 Q1-K1-F6 789 16 LIB3073-011- LIB3073 g1055367 BLASTN 647 1e−150 94 Q1-K1-A12 790 16 LIB3073-007- LIB3073 g1055367 BLASTN 1110 1e−150 98 Q1-K1-B9 791 16 LIB3055-005- LIB3055 g1055367 BLASTN 1877 1e−150 93 Q1-N1-G4 792 16 LIB3073-006- LIB3073 g1055367 BLASTN 1886 1e−150 99 Q1-K1-F5 793 16 LIB3073-022- LIB3073 g1055367 BLASTN 1765 1e−149 94 Q1-K1-B9 794 16 LIB3073-024- LIB3073 g1055367 BLASTN 1768 1e−149 95 Q1-K1-F3 795 16 LIB3073-026- LIB3073 g1055367 BLASTN 1866 1e−149 98 Q1-K1-E6 796 16 LIB3073-025- LIB3073 g1055367 BLASTN 1855 1e−148 98 Q1-K1-F3 797 16 LIB3073-024- LIB3073 g1055367 BLASTN 1630 1e−147 94 Q1-K1-B5 798 16 LIB3053-010- LIB3053 g1055367 BLASTN 1677 1e−147 94 Q1-N1-A2 799 16 LIB3073-007- LIB3073 g1055367 BLASTN 946 1e−146 97 Q1-K1-F1 800 16 LIB3055-008- LIB3055 g1055367 BLASTN 1731 1e−146 93 Q1-N1-E12 801 16 LIB3073-001- LIB3073 g1055367 BLASTN 988 1e−145 97 Q1-K1-B7 802 16 LIB3039-004- LIB3039 g1055367 BLASTN 1817 1e−145 98 Q1-E1-F7 803 16 LIB3053-006- LIB3053 g1055367 BLASTN 1823 1e−145 95 Q1-N1-D9 804 16 LIB3039-021- LIB3039 g1055367 BLASTN 906 1e−143 96 Q1-E1-A3 805 16 LIB3053-001- LIB3053 g1055367 BLASTN 1367 1e−143 91 Q1-B1-D4 806 16 LIB3039-046- LIB3039 g1055367 BLASTN 1567 1e−143 99 Q1-E1-E5 807 16 LIB3073-007- LIB3073 g1055367 BLASTN 1392 1e−142 92 Q1-K1-B2 808 16 LIB3073-023- LIB3073 g1055367 BLASTN 1683 1e−142 88 Q1-K1-C3 809 16 LIB3055-002- LIB3055 g1055367 BLASTN 912 1e−141 90 Q1-B1-E1 810 16 LIB3073-025- LIB3073 g1055367 BLASTN 1769 1e−141 93 Q1-K1-H8 811 16 LIB3039-030- LIB3039 g1055367 BLASTN 1775 1e−141 99 Q1-E1-H9 812 16 LIB3055-008- LIB3055 g1055367 BLASTN 659 1e−140 93 Q1-N1-H4 813 16 LIB3054-011- LIB3054 g1055367 BLASTN 1384 1e−140 90 Q1-N1-A1 814 16 LIB3073-025- LIB3073 g1055367 BLASTN 1758 1e−140 95 Q1-K1-D2 815 16 LIB3073-025- LIB3073 g1055367 BLASTN 1763 1e−140 97 Q1-K1-G3 816 16 LIB3053-002- LIB3053 g1055367 BLASTN 686 1e−139 94 Q1-B1-H2 817 16 LIB3073-013- LIB3073 g1055367 BLASTN 1590 1e−138 96 Q1-K1-F6 818 16 LIB3073-025- LIB3073 g1055367 BLASTN 1643 1e−138 94 Q1-K1-B10 819 16 LIB3073-023- LIB3073 g1055367 BLASTN 1286 1e−137 95 Q1-K1-D3 820 16 LIB3054-011- LIB3054 g1055367 BLASTN 1507 1e−137 98 Q1-N1-G1 821 16 LIB3073-024- LIB3073 g1055367 BLASTN 1135 1e−135 97 Q1-K1-H12 822 16 LIB3039-002- LIB3039 g1055367 BLASTN 1499 1e−135 94 Q1-E1-E5 823 16 LIB3073-026- LIB3073 g1055367 BLASTN 1696 1e−135 94 Q1-K1-E3 824 16 LIB3054-006- LIB3054 g1055367 BLASTN 1593 1e−134 93 Q1-N1-F11 825 16 LIB3028-009- LIB3028 g1055367 BLASTN 1318 1e−133 91 Q1-B1-D4 826 16 LIB3073-026- LIB3073 g1055367 BLASTN 1681 1e−133 99 Q1-K1-A12 827 16 LIB3073-011- LIB3073 g1055367 BLASTN 1213 1e−131 94 Q1-K1-C7 828 16 LIB3054-001- LIB3054 g1055367 BLASTN 1644 1e−130 91 Q1-B1-A6 829 16 LIB3073-002- LIB3073 g1055367 BLASTN 1414 1e−129 92 Q1-K1-A8 830 16 LIB3073-002- LIB3073 g1079735 BLASTN 1120 1e−126 91 Q1-K1-E11 831 16 LIB3040-056- LIB3040 g1055367 BLASTN 1590 1e−126 98 Q1-E1-E11 832 16 LIB3073-025- LIB3073 g1055367 BLASTN 1503 1e−124 98 Q1-K1-G10 833 16 LIB3054-003- LIB3054 g1055367 BLASTN 1262 1e−123 95 Q1-N1-G2 834 16 LIB3073-011- LIB3073 g1055367 BLASTN 1379 1e−122 93 Q1-K1-D5 835 16 LIB3054-011- LIB3054 g1055367 BLASTN 1477 1e−122 91 Q1-N1-C4 836 16 LIB3049-038- LIB3049 g1055367 BLASTN 1353 1e−118 89 Q1-E1-G6 837 16 LIB3039-033- LIB3039 g1055367 BLASTN 1482 1e−117 93 Q1-E1-H12 838 16 LIB3039-031- LIB3039 g1079735 BLASTN 943 1e−111 94 Q1-E1-D2 839 16 LIB3030-004- LIB3030 g1055367 BLASTN 1282 1e−109 96 Q1-B1-A8 840 16 LIB3055-004- LIB3055 g1055367 BLASTN 1142 1e−101 96 Q1-N1-F1 841 16 LIB3053-001- LIB3053 g1055367 BLASTN 724 1e−97 87 Q1-B1-H1 842 16 LIB3054-001- LIB3054 g1055367 BLASTN 868 1e−84 91 Q1-B1-C9 843 16 LIB3073-002- LIB3073 g1079735 BLASTN 917 1e−81 91 Q1-K1-F5 844 16 LIB3073-026- LIB3073 g1055367 BLASTN 797 1e−79 85 Q1-K1-B9 845 16 LIB3039-005- LIB3039 g1079735 BLASTN 897 1e−79 92 Q1-E1-E4 846 16 LIB3054-006- LIB3054 g1055367 BLASTN 839 1e−61 90 Q1-N1-E5 847 16 LIB3055-007- LIB3055 g1055367 BLASTN 620 1e−42 100 Q1-N1-G1 MAIZE PHOSPHOGLYCERATE KINASE 848 -700073531 700073531H1 SATMON007 g21834 BLASTN 324 1e−16 69 849 -700215712 700215712H1 SATMON016 g21272 BLASTX 87 1e−11 66 850 -700220093 700220093H1 SATMON011 g21834 BLASTN 258 1e−31 82 851 -700336084 700336084H1 SATMON019 g218038 BLASTN 389 1e−21 65 852 -700442802 700442802H1 SATMON026 g21832 BLASTN 298 1e−60 90 853 -700611444 700611444H1 SATMON022 g21832 BLASTN 831 1e−60 82 854 -700623464 700623464H1 SATMON034 g21834 BLASTN 261 1e−24 74 855 -700805505 700805505H1 SATMON036 g21834 BLASTN 512 1e−33 87 856 16294 700101571H1 SATMON009 g21832 BLASTN 891 1e−65 82 857 16294 700218404H1 SATMON016 g21832 BLASTN 595 1e−53 82 858 16294 700093042H1 SATMON008 g1022803 BLASTX 146 1e−13 88 859 16294 700093371H1 SATMON008 g1022803 BLASTX 133 1e−11 88 860 2232 700098158H1 SATMON009 g21832 BLASTN 1303 1e−99 89 861 2232 700210258H1 SATMON016 g21832 BLASTN 1246 1e−95 87 862 2232 700099304H1 SATMON009 g21832 BLASTN 1235 1e−94 87 863 2232 700100457H1 SATMON009 g21832 BLASTN 1240 1e−94 89 864 2232 700097084H1 SATMON009 g21832 BLASTN 1242 1e−94 87 865 2232 700097420H1 SATMON009 g21832 BLASTN 1146 1e−86 88 866 2232 700216186H1 SATMON016 g21832 BLASTN 1128 1e−85 89 867 2232 700098880H1 SATMON009 g21832 BLASTN 1116 1e−84 83 868 2232 700098821H1 SATMON009 g21832 BLASTN 1121 1e−84 83 869 2232 700041819H1 SATMON004 g21832 BLASTN 1081 1e−81 88 870 2232 700210748H1 SATMON016 g21832 BLASTN 1069 1e−80 84 871 2232 700097556H1 SATMON009 g21832 BLASTN 1056 1e−79 84 872 2232 700578230H1 SATMON031 g21832 BLASTN 1060 1e−79 90 873 2232 700580556H1 SATMON031 g21832 BLASTN 1045 1e−78 86 874 2232 700044785H1 SATMON004 g21832 BLASTN 1050 1e−78 88 875 2232 700041775H1 SATMON004 g21832 BLASTN 1035 1e−77 88 876 2232 700045331H1 SATMON004 g21832 BLASTN 996 1e−74 87 877 2232 700046021H1 SATMON004 g21832 BLASTN 1003 1e−74 84 878 2232 700344283H1 SATMON021 g21832 BLASTN 922 1e−73 91 879 2232 700242032H1 SATMON010 g21832 BLASTN 986 1e−73 86 880 2232 700044688H1 SATMON004 g21832 BLASTN 991 1e−73 89 881 2232 700053496H1 SATMON009 g21832 BLASTN 958 1e−71 83 882 2232 700043267H1 SATMON004 g21832 BLASTN 941 1e−69 84 883 2232 700577778H1 SATMON031 g21832 BLASTN 922 1e−68 83 884 2232 700045845H1 SATMON004 g21832 BLASTN 856 1e−62 82 885 2232 700439945H1 SATMON026 g21832 BLASTN 803 1e−58 85 886 2232 700240633H1 SATMON010 g21832 BLASTN 753 1e−53 83 887 2232 700424659H1 SATMONN01 g21832 BLASTN 429 1e−39 80 888 2232 700042421H1 SATMON004 g21832 BLASTN 447 1e−28 93 889 2769 700100967H1 SATMON009 g21834 BLASTN 481 1e−34 90 890 66 700209994H1 SATMON016 g21834 BLASTN 658 1e−100 85 891 66 700103176H1 SATMON010 g21834 BLASTN 1178 1e−97 89 892 66 700262312H1 SATMON017 g21834 BLASTN 1264 1e−96 90 893 66 700103182H1 SATMON010 g21834 BLASTN 1256 1e−95 89 894 66 700216542H1 SATMON016 g21834 BLASTN 1233 1e−94 89 895 66 700104446H1 SATMON010 g21834 BLASTN 1231 1e−93 91 896 66 700236428H1 SATMON010 g21834 BLASTN 1200 1e−91 92 897 66 700257977H1 SATMON017 g21834 BLASTN 1011 1e−88 91 898 66 700072449H1 SATMON007 g21834 BLASTN 1103 1e−88 93 899 66 700089147H1 SATMON011 g21834 BLASTN 1164 1e−88 81 900 66 700208306H1 SATMON016 g21834 BLASTN 1170 1e−88 94 901 66 700104358H1 SATMON010 g21834 BLASTN 1141 1e−86 88 902 66 700266788H1 SATMON017 g21834 BLASTN 1131 1e−85 86 903 66 700219877H1 SATMON011 g21834 BLASTN 1136 1e−85 90 904 66 700083123H1 SATMON011 g21834 BLASTN 1059 1e−84 94 905 66 700087896H1 SATMON011 g21834 BLASTN 1059 1e−84 94 906 66 700265143H1 SATMON017 g21834 BLASTN 1044 1e−83 94 907 66 700097447H1 SATMON009 g21834 BLASTN 1032 1e−82 93 908 66 700072364H1 SATMON007 g21834 BLASTN 1033 1e−82 93 909 66 700099968H1 SATMON009 g21834 BLASTN 1034 1e−82 93 910 66 700075887H1 SATMON007 g21834 BLASTN 1041 1e−82 92 911 66 700027135H1 SATMON003 g21834 BLASTN 1003 1e−81 90 912 66 700097469H1 SATMON009 g21834 BLASTN 1024 1e−81 93 913 66 700267426H1 SATMON017 g21834 BLASTN 1025 1e−81 93 914 66 700215049H1 SATMON016 g21834 BLASTN 1074 1e−80 90 915 66 700619962H1 SATMON034 g21834 BLASTN 733 1e−79 93 916 66 700332089H1 SATMON019 g21834 BLASTN 997 1e−79 94 917 66 700351610H1 SATMON023 g21834 BLASTN 998 1e−79 94 918 66 700075430H1 SATMON007 g21834 BLASTN 1003 1e−79 93 919 66 700092332H1 SATMON008 g21834 BLASTN 1059 1e−79 94 920 66 700405456H1 SATMON029 g21834 BLASTN 858 1e−78 85 921 66 700798970H1 SATMON036 g21834 BLASTN 962 1e−78 89 922 66 700028644H1 SATMON003 g21834 BLASTN 1043 1e−78 88 923 66 700092404H1 SATMON008 g21834 BLASTN 1050 1e−78 81 924 66 700093208H1 SATMON008 g21834 BLASTN 1052 1e−78 81 925 66 700073284H1 SATMON007 g21834 BLASTN 977 1e−77 94 926 66 700620115H1 SATMON034 g21834 BLASTN 773 1e−76 94 927 66 700262412H1 SATMON017 g21834 BLASTN 961 1e−76 93 928 66 700025960H1 SATMON003 g21834 BLASTN 962 1e−76 94 929 66 700549575H1 SATMON022 g21834 BLASTN 996 1e−76 88 930 66 700579774H1 SATMON031 g21834 BLASTN 697 1e−75 78 931 66 700264301H1 SATMON017 g21834 BLASTN 839 1e−75 92 932 66 700333669H1 SATMON019 g21834 BLASTN 904 1e−75 91 933 66 700268190H1 SATMON017 g21834 BLASTN 947 1e−75 94 934 66 700050952H1 SATMON003 g21834 BLASTN 954 1e−75 93 935 66 700349338H1 SATMON023 g21834 BLASTN 762 1e−74 89 936 66 700282206H1 SATMON023 g21834 BLASTN 862 1e−74 88 937 66 700344952H1 SATMON021 g21834 BLASTN 926 1e−74 87 938 66 700043612H1 SATMON004 g21834 BLASTN 916 1e−73 92 939 66 700221930H1 SATMON011 g21834 BLASTN 959 1e−73 81 940 66 700204594H1 SATMON003 g21834 BLASTN 924 1e−72 83 941 66 700099108H1 SATMON009 g21834 BLASTN 975 1e−72 82 942 66 700570931H1 SATMON030 g21834 BLASTN 407 1e−70 89 943 66 700077368H1 SATMON007 g21834 BLASTN 888 1e−70 94 944 66 700044806H1 SATMON004 g21834 BLASTN 892 1e−70 94 945 66 700217737H1 SATMON016 g21834 BLASTN 895 1e−70 94 946 66 700805779H1 SATMON036 g21834 BLASTN 898 1e−70 94 947 66 700211352H1 SATMON016 g21834 BLASTN 903 1e−70 90 948 66 700088868H1 SATMON011 g21834 BLASTN 947 1e−70 88 949 66 700348871H1 SATMON023 g21834 BLASTN 953 1e−70 86 950 66 700243521H1 SATMON010 g21834 BLASTN 874 1e−69 94 951 66 700350430H1 SATMON023 g21834 BLASTN 889 1e−69 94 952 66 700150315H1 SATMON007 g21834 BLASTN 945 1e−69 93 953 66 700350880H1 SATMON023 g21834 BLASTN 424 1e−68 88 954 66 700093908H1 SATMON008 g21834 BLASTN 821 1e−68 87 955 66 700076677H1 SATMON007 g21834 BLASTN 865 1e−68 95 956 66 700091547H1 SATMON011 g21834 BLASTN 867 1e−68 94 957 66 700458384H1 SATMON029 g21834 BLASTN 868 1e−68 93 958 66 700222907H1 SATMON011 g21834 BLASTN 879 1e−68 94 959 66 700618842H1 SATMON034 g21834 BLASTN 526 1e−67 94 960 66 700339442H1 SATMON020 g21834 BLASTN 771 1e−67 82 961 66 700240067H1 SATMON010 g21834 BLASTN 913 1e−67 82 962 66 700266865H1 SATMON017 g21834 BLASTN 907 1e−66 88 963 66 700451654H1 SATMON028 g21834 BLASTN 461 1e−65 93 964 66 700087164H1 SATMON011 g21834 BLASTN 644 1e−65 88 965 66 700343701H1 SATMON021 g21834 BLASTN 699 1e−65 88 966 66 700800530H1 SATMON036 g21834 BLASTN 708 1e−65 94 967 66 700441116H1 SATMON026 g21834 BLASTN 440 1e−64 87 968 66 700094769H1 SATMON008 g21834 BLASTN 779 1e−63 92 969 66 700457925H1 SATMON029 g21834 BLASTN 785 1e−63 85 970 66 700571062H1 SATMON030 g21834 BLASTN 826 1e−63 95 971 66 700258601H1 SATMON017 g21834 BLASTN 708 1e−62 95 972 66 700579874H1 SATMON031 g21834 BLASTN 773 1e−62 83 973 66 700454374H1 SATMON029 g21834 BLASTN 825 1e−62 91 974 66 700094413H1 SATMON008 g21834 BLASTN 668 1e−61 92 975 66 700072959H1 SATMON007 g21834 BLASTN 701 1e−61 95 976 66 700161495H1 SATMON012 g21834 BLASTN 765 1e−61 85 977 66 700153976H1 SATMON007 g21834 BLASTN 778 1e−61 95 978 66 700156134H2 SATMON007 g21834 BLASTN 778 1e−61 95 979 66 700043126H1 SATMON004 g21834 BLASTN 845 1e−61 83 980 66 700159683H1 SATMON012 g21834 BLASTN 845 1e−61 82 981 66 700157671H1 SATMON012 g21834 BLASTN 835 1e−60 83 982 66 700549008H1 SATMON022 g21834 BLASTN 691 1e−59 81 983 66 700104417H1 SATMON010 g21834 BLASTN 756 1e−59 91 984 66 700094721H1 SATMON008 g21834 BLASTN 815 1e−59 94 985 66 700611620H1 SATMON022 g21834 BLASTN 818 1e−59 82 986 66 700455655H1 SATMON029 g21834 BLASTN 357 1e−58 92 987 66 700549606H1 SATMON022 g21834 BLASTN 425 1e−58 79 988 66 700165361H1 SATMON013 g21834 BLASTN 748 1e−58 95 989 66 700076792H1 SATMON007 g21834 BLASTN 749 1e−58 94 990 66 700048731H1 SATMON003 g21834 BLASTN 808 1e−58 78 991 66 700168266H1 SATMON013 g21834 BLASTN 811 1e−58 82 992 66 700045117H1 SATMON004 g21834 BLASTN 812 1e−58 80 993 66 700209421H1 SATMON016 g21834 BLASTN 813 1e−58 95 994 66 700806575H1 SATMON036 g21834 BLASTN 736 1e−57 94 995 66 700456047H1 SATMON029 g21834 BLASTN 796 1e−57 81 996 66 700623432H1 SATMON034 g21834 BLASTN 801 1e−57 91 997 66 700569724H1 SATMON030 g21834 BLASTN 525 1e−56 80 998 66 700220377H1 SATMON011 g21834 BLASTN 732 1e−56 83 999 66 700336275H1 SATMON019 g21834 BLASTN 621 1e−55 87 1000 66 700151932H1 SATMON007 g21834 BLASTN 711 1e−55 94 1001 66 700258488H1 SATMON017 g21834 BLASTN 693 1e−54 94 1002 66 700333184H1 SATMON019 g21834 BLASTN 708 1e−54 93 1003 66 700236590H1 SATMON010 g21834 BLASTN 759 1e−54 94 1004 66 700440409H1 SATMON026 g21834 BLASTN 392 1e−53 83 1005 66 700615448H1 SATMON033 g21834 BLASTN 402 1e−53 91 1006 66 700023196H1 SATMON003 g21834 BLASTN 738 1e−52 80 1007 66 700577864H1 SATMON031 g1161601 BLASTN 399 1e−51 76 1008 66 700073368H1 SATMON007 g1161601 BLASTN 429 1e−51 78 1009 66 700344214H1 SATMON021 g21834 BLASTN 400 1e−49 86 1010 66 700019682H1 SATMON001 g21834 BLASTN 694 1e−49 83 1011 66 700153175H1 SATMON007 g21834 BLASTN 701 1e−49 79 1012 66 700236532H1 SATMON010 g1161601 BLASTN 435 1e−48 76 1013 66 700263441H1 SATMON017 g21834 BLASTN 688 1e−48 91 1014 66 700473818H1 SATMON025 g21834 BLASTN 667 1e−46 92 1015 66 700471618H1 SATMON025 g21834 BLASTN 591 1e−45 95 1016 66 700612632H1 SATMON033 g21834 BLASTN 591 1e−45 91 1017 66 700266580H1 SATMON017 g21834 BLASTN 455 1e−43 84 1018 66 700474244H1 SATMON025 g21834 BLASTN 563 1e−43 92 1019 66 700195129H1 SATMON014 g21834 BLASTN 627 1e−43 86 1020 66 700104765H1 SATMON010 g21834 BLASTN 627 1e−43 86 1021 66 700029314H1 SATMON003 g21834 BLASTN 627 1e−43 86 1022 66 700041618H1 SATMON004 g21834 BLASTN 627 1e−43 86 1023 66 700050511H1 SATMON003 g21834 BLASTN 618 1e−42 86 1024 66 700195775H1 SATMON014 g21834 BLASTN 620 1e−42 86 1025 66 700195425H1 SATMON014 g21834 BLASTN 604 1e−41 75 1026 66 700440268H1 SATMON026 g21834 BLASTN 608 1e−41 86 1027 66 700160639H1 SATMON012 g21834 BLASTN 609 1e−41 85 1028 66 700617741H1 SATMON033 g2982312 BLASTN 402 1e−40 77 1029 66 700578506H1 SATMON031 g21834 BLASTN 580 1e−39 82 1030 66 700618491H2 SATMON033 g21834 BLASTN 591 1e−39 85 1031 66 700803231H1 SATMON036 g21834 BLASTN 455 1e−38 86 1032 66 700195008H1 SATMON014 g21834 BLASTN 559 1e−37 80 1033 66 700257337H1 SATMON017 g21834 BLASTN 463 1e−35 90 1034 66 700153701H1 SATMON007 g21834 BLASTN 529 1e−35 86 1035 66 700458028H1 SATMON029 g21834 BLASTN 270 1e−33 85 1036 66 700350024H1 SATMON023 g21834 BLASTN 387 1e−33 83 1037 66 700150871H1 SATMON007 g21834 BLASTN 431 1e−32 90 1038 66 700804078H1 SATMON036 g21834 BLASTN 491 1e−32 83 1039 66 700267617H1 SATMON017 g21834 BLASTN 423 1e−31 93 1040 66 701165809H1 SATMONN04 g21834 BLASTN 279 1e−26 83 1041 66 700552775H1 SATMON022 g21834 BLASTN 429 1e−25 79 1042 66 700616491H1 SATMON033 g21835 BLASTX 89 1e−16 82 1043 66 700450825H1 SATMON028 g21834 BLASTN 240 1e−16 90 1044 66 700334736H1 SATMON019 g1161602 BLASTX 126 1e−14 76 1045 66 700202264H1 SATMON003 g21834 BLASTN 214 1e−14 92 1046 66 700583352H1 SATMON031 g1161602 BLASTX 117 1e−9 100 1047 66 700802543H1 SATMON036 g21834 BLASTN 233 1e−9 94 1048 66 700018689H1 SATMON001 g3309631 BLASTX 103 1e−8 89 1049 -L30621557 LIB3062-018- LIB3062 g313266 BLASTN 776 1e−60 79 Q1-K1-F2 1050 -L30624706 LIB3062-049- LIB3062 g21832 BLASTN 906 1e−102 79 Q1-K1-H7 1051 -L30672623 LIB3067-004- LIB3067 g21834 BLASTN 571 1e−38 89 Q1-K1-A5 1052 16294 LIB3078-050- LIB3078 g21832 BLASTN 747 1e−60 83 Q1-K1-D12 1053 16294 LIB3078-049- LIB3078 g21832 BLASTN 207 1e−14 84 Q1-K1-H7 1054 2232 LIB3078-002- LIB3078 g21832 BLASTN 1606 1e−125 87 Q1-K1-C4 1055 2232 LIB36-001- LIB36 g21832 BLASTN 1293 1e−123 84 Q1-E1-B11 1056 2232 LIB36-009- LIB36 g21832 BLASTN 1591 1e−123 88 Q1-E1-G7 1057 2232 LIB3078-003- LIB3078 g21832 BLASTN 1429 1e−117 88 Q1-K1-G10 1058 2232 LIB36-008- LIB36 g21832 BLASTN 1340 1e−110 84 Q1-E1-H5 1059 2232 LIB3078-014- LIB3078 g21832 BLASTN 1422 1e−109 86 Q1-K1-F7 1060 2232 LIB36-017- LIB36 g21832 BLASTN 1230 1e−99 84 Q1-E1-D8 1061 2232 LIB3078-052- LIB3078 g21832 BLASTN 1045 1e−96 79 Q1-K1-F3 1062 2232 11-LIB189- LIB189 g21832 BLASTN 912 1e−72 81 015-Q1-E1- C11 1063 2769 LIB143-014- LIB143 g21834 BLASTN 199 1e−10 82 Q1-E1-A9 1064 66 LIB3060-012- LIB3060 g21834 BLASTN 1691 1e−132 87 Q1-K1-H11 1065 66 LIB3069-045- LIB3069 g21834 BLASTN 1224 1e−124 92 Q1-K1-C4 1066 66 LIB3059-047- LIB3059 g21834 BLASTN 1338 1e−115 92 Q1-K1-A8 1067 66 LIB189-027- LIB189 g21834 BLASTN 1485 1e−115 88 Q1-E1-D10 1068 66 LIB83-006- LIB83 g21834 BLASTN 1148 1e−114 80 Q1-E1-F2 1069 66 LIB3060-017- LIB3060 g21834 BLASTN 1187 1e−113 79 Q1-K1-G5 1070 66 LIB143-011- LIB143 g21834 BLASTN 1412 1e−113 93 Q1-E1-B6 1071 66 LIB3059-006- LIB3059 g21834 BLASTN 1452 1e−112 82 Q1-K1-A4 1072 66 LIB143-011- LIB143 g21834 BLASTN 1460 1e−112 89 Q1-E1-E3 1073 66 LIB3059-041- LIB3059 g21834 BLASTN 1441 1e−111 82 Q1-K1-D2 1074 66 LIB3079-002- LIB3079 g21834 BLASTN 977 1e−101 85 Q1-K1-H3 1075 66 LIB3061-049- LIB3061 g21834 BLASTN 1247 1e−99 79 Q1-K1-G6 1076 66 LIB3059-038- LIB3059 g21834 BLASTN 1094 1e−97 81 Q1-K1-H8 1077 66 LIB3062-017- LIB3062 g21834 BLASTN 1236 1e−97 93 Q1-K1-D10 1078 66 LIB3059-022- LIB3059 g21834 BLASTN 982 1e−94 82 Q1-K1-C10 1079 66 LIB3059-027- LIB3059 g21834 BLASTN 1029 1e−89 78 Q1-K1-C7 1080 66 LIB3060-011- LIB3060 g21834 BLASTN 1139 1e−86 81 Q1-K1-A10 1081 66 LIB3067-046- LIB3067 g21834 BLASTN 967 1e−82 75 Q1-K1-A9 1082 66 LIB3061-049- LIB3061 g21834 BLASTN 950 1e−79 91 Q1-K1-G5 1083 66 LIB3067-007- LIB3067 g21834 BLASTN 979 1e−72 81 Q1-K1-E6 1084 66 LIB143-052- LIB143 g1161601 BLASTN 528 1e−69 77 Q1-E1-C5 1085 66 LIB143-068- LIB143 g21834 BLASTN 879 1e−67 90 Q1-E1-H4 1086 66 LIB3069-052- LIB3069 g21834 BLASTN 843 1e−65 93 Q1-K1-E12 1087 66 LIB3059-012- LIB3059 g21834 BLASTN 611 1e−62 82 Q1-K1-B7 1088 66 LIB3078-056- LIB3078 g1161601 BLASTN 467 1e−58 77 Q1-K1-D5 1089 66 LIB3062-035- LIB3062 g21834 BLASTN 320 1e−47 81 Q1-K1-H2 1090 66 LIB3069-045- LIB3069 g21834 BLASTN 627 1e−41 86 Q1-K1-D11 SOYBEAN PHOSPHOGLYCERATE KINASE 1091 -700561750 700561750H1 SOYMON002 g1161602 BLASTX 98 1e−16 90 1092 -700655290 700655290H1 SOYMON004 g1177860 BLASTX 58 1e−14 67 1093 -700846548 700846548H1 SOYMON021 g21833 BLASTX 158 1e−14 83 1094 -700867263 700867263H1 SOYMON016 g1161602 BLASTX 132 1e−11 85 1095 -700989319 700989319H1 SOYMON011 g1022803 BLASTX 99 1e−15 72 1096 -700998533 700998533H1 SOYMON018 g2257597 BLASTN 406 1e−25 75 1097 -701104514 701104514H1 SOYMON036 g21272 BLASTX 169 1e−17 78 1098 -701108251 701108251H1 SOYMON036 g21271 BLASTN 561 1e−37 83 1099 16 701045420H1 SOYMON032 g2257597 BLASTN 937 1e−69 92 1100 16 700979939H1 SOYMON009 g21271 BLASTN 921 1e−67 82 1101 16 700962832H1 SOYMON022 g1022804 BLASTN 882 1e−64 82 1102 16 700648009H1 SOYMON003 g21271 BLASTN 859 1e−62 75 1103 16 700901512H1 SOYMON027 g1022804 BLASTN 840 1e−61 79 1104 16 701120901H1 SOYMON037 g21271 BLASTN 816 1e−59 76 1105 16 700731242H1 SOYMON009 g1022804 BLASTN 803 1e−58 80 1106 16 700995275H1 SOYMON011 g1022804 BLASTN 791 1e−57 84 1107 16 700566593H1 SOYMON002 g1161601 BLASTN 795 1e−57 75 1108 16 701152346H1 SOYMON031 g1161599 BLASTN 636 1e−56 78 1109 16 700999851H1 SOYMON018 g21271 BLASTN 769 1e−55 83 1110 16 700877067H1 SOYMON018 g1022804 BLASTN 774 1e−55 82 1111 16 700743313H1 SOYMON012 g1022804 BLASTN 765 1e−54 84 1112 16 700605425H2 SOYMON004 g1161601 BLASTN 747 1e−53 75 1113 16 700846107H1 SOYMON021 g1161601 BLASTN 750 1e−53 76 1114 16 700755167H1 SOYMON014 g1022804 BLASTN 730 1e−52 80 1115 16 700986996H1 SOYMON009 g21271 BLASTN 736 1e−52 73 1116 16 700873077H1 SOYMON018 g1161601 BLASTN 721 1e−51 75 1117 16 700995849H1 SOYMON011 g1161601 BLASTN 698 1e−49 76 1118 16 700754326H1 SOYMON014 g1022804 BLASTN 301 1e−48 84 1119 16 701063449H1 SOYMON033 g1161601 BLASTN 685 1e−48 75 1120 16 700906269H1 SOYMON022 g1161601 BLASTN 687 1e−48 73 1121 16 701121153H1 SOYMON037 g1161601 BLASTN 669 1e−46 76 1122 16 700750611H1 SOYMON014 g1161601 BLASTN 653 1e−45 75 1123 16 701051356H1 SOYMON032 g1161601 BLASTN 636 1e−44 74 1124 16 701040938H1 SOYMON029 g1161601 BLASTN 637 1e−44 76 1125 16 701141327H1 SOYMON038 g1161601 BLASTN 638 1e−44 76 1126 16 701041022H1 SOYMON029 g1161601 BLASTN 642 1e−44 76 1127 16 700560223H1 SOYMON001 g1161601 BLASTN 548 1e−42 77 1128 16 701069688H1 SOYMON034 g1161601 BLASTN 610 1e−42 74 1129 16 700868226H1 SOYMON016 g1161601 BLASTN 593 1e−40 75 1130 16 700867389H1 SOYMON016 g1022804 BLASTN 476 1e−39 82 1131 16 700792652H1 SOYMON017 g1161601 BLASTN 574 1e−39 75 1132 16 701206846H1 SOYMON035 g1161601 BLASTN 576 1e−39 78 1133 16 700966925H1 SOYMON029 g1161601 BLASTN 577 1e−39 76 1134 16 700676242H1 SOYMON007 g1161601 BLASTN 579 1e−39 75 1135 16 700982087H1 SOYMON009 g1161601 BLASTN 533 1e−38 76 1136 16 701206122H1 SOYMON035 g1161601 BLASTN 541 1e−38 76 1137 16 700561967H1 SOYMON002 g1161601 BLASTN 566 1e−38 78 1138 16 701038580H1 SOYMON029 g1161601 BLASTN 568 1e−38 78 1139 16 700831261H1 SOYMON019 g21834 BLASTN 569 1e−38 77 1140 16 700909538H1 SOYMON022 g1161601 BLASTN 475 1e−37 75 1141 16 701109480H1 SOYMON036 g1161601 BLASTN 551 1e−37 76 1142 16 700754158H1 SOYMON014 g1161601 BLASTN 552 1e−37 74 1143 16 701138938H1 SOYMON038 g1161601 BLASTN 558 1e−37 77 1144 16 700728645H1 SOYMON009 g1161601 BLASTN 559 1e−37 77 1145 16 701037523H1 SOYMON029 g1161601 BLASTN 560 1e−37 73 1146 16 700746355H1 SOYMON013 g1161601 BLASTN 544 1e−36 81 1147 16 700753250H1 SOYMON014 g1161601 BLASTN 544 1e−36 81 1148 16 700742113H1 SOYMON012 g1022804 BLASTN 546 1e−36 85 1149 16 700754067H1 SOYMON014 g1161599 BLASTN 547 1e−36 76 1150 16 701060528H1 SOYMON033 g1161601 BLASTN 548 1e−36 77 1151 16 701002709H2 SOYMON019 g1161601 BLASTN 549 1e−36 76 1152 16 700958261H1 SOYMON022 g1161601 BLASTN 549 1e−36 76 1153 16 701212692H1 SOYMON035 g1161601 BLASTN 549 1e−36 76 1154 16 701129677H1 SOYMON037 g1161601 BLASTN 301 1e−35 75 1155 16 700755130H1 SOYMON014 g1161601 BLASTN 526 1e−35 80 1156 16 700855106H1 SOYMON023 g1161601 BLASTN 528 1e−35 75 1157 16 700672102H1 SOYMON006 g1161601 BLASTN 530 1e−35 75 1158 16 700985023H1 SOYMON009 g1161601 BLASTN 530 1e−35 73 1159 16 700561815H1 SOYMON002 g1161601 BLASTN 531 1e−35 77 1160 16 700650261H1 SOYMON003 g1161601 BLASTN 535 1e−35 81 1161 16 701155840H1 SOYMON031 g1161601 BLASTN 535 1e−35 81 1162 16 701011614H1 SOYMON019 g1161601 BLASTN 535 1e−35 75 1163 16 700756614H1 SOYMON014 g1161601 BLASTN 536 1e−35 80 1164 16 700753242H1 SOYMON014 g1161601 BLASTN 537 1e−35 77 1165 16 701062065H1 SOYMON033 g1161601 BLASTN 343 1e−34 76 1166 16 700734980H1 SOYMON010 g1161601 BLASTN 372 1e−34 78 1167 16 700894670H1 SOYMON024 g1161601 BLASTN 515 1e−34 80 1168 16 701004704H1 SOYMON019 g1161601 BLASTN 521 1e−34 80 1169 16 701125560H1 SOYMON037 g1161601 BLASTN 504 1e−33 81 1170 16 700673963H1 SOYMON007 g1161601 BLASTN 512 1e−33 80 1171 16 700664685H1 SOYMON005 g218212 BLASTN 417 1e−32 71 1172 16 700756635H1 SOYMON014 g1161601 BLASTN 498 1e−32 66 1173 16 701066933H1 SOYMON034 g1161601 BLASTN 487 1e−31 80 1174 16 701156137H1 SOYMON031 g1161601 BLASTN 412 1e−30 81 1175 16 701043044H1 SOYMON029 g1161601 BLASTN 456 1e−29 79 1176 16 700832331H1 SOYMON019 g1161601 BLASTN 387 1e−28 79 1177 16 701046244H1 SOYMON032 g1161601 BLASTN 451 1e−28 81 1178 16 700555893H1 SOYMON001 g1161602 BLASTX 153 1e−26 81 1179 16 700999829H1 SOYMON018 g21271 BLASTN 355 1e−26 73 1180 16 701142924H2 SOYMON038 g1161601 BLASTN 428 1e−26 81 1181 16 701156281H1 SOYMON031 g1161601 BLASTN 428 1e−26 81 1182 16 701015402H1 SOYMON019 g1161602 BLASTX 126 1e−23 78 1183 16 700870906H1 SOYMON018 g1161602 BLASTX 108 1e−19 85 1184 16 701060159H1 SOYMON033 g1161601 BLASTN 348 1e−18 72 1185 16 700830018H1 SOYMON019 g1161602 BLASTX 116 1e−16 73 1186 16 700910043H1 SOYMON022 g1161601 BLASTN 328 1e−16 75 1187 16 701043760H1 SOYMON032 g1161602 BLASTX 154 1e−14 83 1188 16 700845883H1 SOYMON021 g1022805 BLASTX 86 1e−13 77 1189 16 700967838H1 SOYMON033 g1161602 BLASTX 87 1e−11 59 1190 16 700731857H1 SOYMON010 g21835 BLASTX 71 1e−10 58 1191 16 701064594H1 SOYMON034 g1161602 BLASTX 125 1e−10 86 1192 16 701062162H1 SOYMON033 g1161599 BLASTN 255 1e−10 72 1193 1699 700560995H1 SOYMON001 g1022804 BLASTN 986 1e−73 82 1194 1699 700562380H1 SOYMON002 g1022804 BLASTN 954 1e−70 82 1195 1699 700985880H1 SOYMON009 g1161599 BLASTN 957 1e−70 82 1196 1699 700560287H1 SOYMON001 g1022802 BLASTN 924 1e−68 80 1197 1699 700963530H1 SOYMON022 g3328121 BLASTN 886 1e−65 80 1198 1699 700875947H1 SOYMON018 g1161599 BLASTN 862 1e−63 83 1199 1699 701000877H1 SOYMON018 g3328121 BLASTN 871 1e−63 78 1200 1699 700875149H1 SOYMON018 g1161599 BLASTN 854 1e−62 82 1201 1699 700562040H1 SOYMON002 g1022804 BLASTN 589 1e−60 82 1202 1699 700988386H1 SOYMON009 g1022804 BLASTN 831 1e−60 80 1203 1699 700684389H1 SOYMON008 g3328121 BLASTN 834 1e−60 81 1204 1699 700561801H1 SOYMON002 g1161599 BLASTN 769 1e−59 77 1205 1699 700898022H1 SOYMON027 g1022802 BLASTN 817 1e−59 80 1206 1699 700790662H2 SOYMON011 g1161599 BLASTN 806 1e−58 82 1207 1699 700684507H1 SOYMON008 g1022802 BLASTN 609 1e−57 80 1208 1699 700844926H1 SOYMON021 g1022802 BLASTN 777 1e−56 81 1209 1699 700875409H1 SOYMON018 g21271 BLASTN 585 1e−55 80 1210 1699 700677812H1 SOYMON007 g21271 BLASTN 776 1e−55 82 1211 1699 701133849H1 SOYMON038 g21832 BLASTN 759 1e−54 80 1212 1699 700978393H1 SOYMON009 g21271 BLASTN 440 1e−53 82 1213 1699 700741608H1 SOYMON012 g3328121 BLASTN 669 1e−53 79 1214 1699 700741228H1 SOYMON012 g1022804 BLASTN 753 1e−53 81 1215 1699 700562038H1 SOYMON002 g21271 BLASTN 662 1e−52 82 1216 1699 700740204H1 SOYMON012 g3328121 BLASTN 730 1e−52 81 1217 1699 700740733H1 SOYMON012 g1161599 BLASTN 662 1e−51 80 1218 1699 700685870H1 SOYMON008 g1022802 BLASTN 720 1e−51 81 1219 1699 700554310H1 SOYMON001 g1161599 BLASTN 558 1e−49 76 1220 1699 700863147H1 SOYMON023 g21832 BLASTN 704 1e−49 83 1221 1699 700991401H1 SOYMON011 g3328121 BLASTN 591 1e−48 80 1222 1699 700998332H1 SOYMON018 g1022802 BLASTN 678 1e−47 81 1223 1699 700945115H1 SOYMON024 g21271 BLASTN 408 1e−46 77 1224 1699 700556386H1 SOYMON001 g21271 BLASTN 615 1e−46 81 1225 1699 700566403H1 SOYMON002 g21271 BLASTN 667 1e−46 80 1226 1699 700683958H1 SOYMON008 g1161599 BLASTN 299 1e−45 83 1227 1699 700686245H1 SOYMON008 g1022802 BLASTN 456 1e−40 84 1228 1699 700787536H1 SOYMON011 g1161599 BLASTN 581 1e−39 81 1229 1699 700740635H1 SOYMON012 g1022804 BLASTN 363 1e−38 84 1230 1699 700875038H1 SOYMON018 g1161599 BLASTN 551 1e−37 81 1231 1699 700677613H1 SOYMON007 g3328121 BLASTN 552 1e−37 83 1232 1699 700683146H1 SOYMON008 g21834 BLASTN 467 1e−29 82 1233 182 700652503H1 SOYMON003 g2257597 BLASTN 861 1e−102 87 1234 182 700653271H1 SOYMON003 g2257597 BLASTN 1303 1e−102 92 1235 182 700653809H1 SOYMON003 g2257597 BLASTN 1303 1e−102 92 1236 182 700653270H1 SOYMON003 g2257597 BLASTN 1303 1e−102 92 1237 182 700653817H1 SOYMON003 g2257597 BLASTN 1289 1e−101 91 1238 182 701105168H1 SOYMON036 g2257597 BLASTN 1219 1e−93 91 1239 182 701045331H1 SOYMON032 g2257597 BLASTN 1194 1e−91 91 1240 182 701049149H1 SOYMON032 g2257597 BLASTN 1162 1e−88 90 1241 182 700661992H1 SOYMON005 g2257597 BLASTN 499 1e−85 86 1242 182 701051265H1 SOYMON032 g2257597 BLASTN 1119 1e−85 91 1243 182 701058557H1 SOYMON033 g2257597 BLASTN 893 1e−83 88 1244 182 700956835H1 SOYMON022 g2257597 BLASTN 1102 1e−83 91 1245 182 701054480H1 SOYMON032 g2257597 BLASTN 918 1e−82 87 1246 182 700903222H1 SOYMON022 g2257597 BLASTN 1074 1e−81 90 1247 182 700959058H1 SOYMON022 g2257597 BLASTN 1078 1e−81 91 1248 182 701105272H1 SOYMON036 g2257597 BLASTN 1081 1e−81 89 1249 182 701058567H1 SOYMON033 g2257597 BLASTN 617 1e−80 91 1250 182 701206133H1 SOYMON035 g2257597 BLASTN 1068 1e−80 88 1251 182 701061140H1 SOYMON033 g2257597 BLASTN 556 1e−79 87 1252 182 700749775H1 SOYMON013 g2257597 BLASTN 1054 1e−79 88 1253 182 700946208H1 SOYMON024 g2257597 BLASTN 1056 1e−79 87 1254 182 700952526H1 SOYMON022 g2257597 BLASTN 1027 1e−77 89 1255 182 700902915H1 SOYMON022 g2257597 BLASTN 1028 1e−77 90 1256 182 700739757H1 SOYMON012 g2257597 BLASTN 1029 1e−77 90 1257 182 700685033H1 SOYMON008 g2257597 BLASTN 1034 1e−77 89 1258 182 700890918H1 SOYMON024 g2257597 BLASTN 1017 1e−76 90 1259 182 700849869H1 SOYMON021 g2257597 BLASTN 1006 1e−75 91 1260 182 701132415H1 SOYMON038 g2257597 BLASTN 521 1e−74 89 1261 182 700835725H1 SOYMON019 g2257597 BLASTN 572 1e−74 88 1262 182 701125828H1 SOYMON037 g2257597 BLASTN 988 1e−74 89 1263 182 700891372H1 SOYMON024 g2257597 BLASTN 967 1e−72 90 1264 182 700898167H1 SOYMON027 g2257597 BLASTN 967 1e−72 87 1265 182 700891730H1 SOYMON024 g2257597 BLASTN 941 1e−70 88 1266 182 700901850H1 SOYMON027 g2257597 BLASTN 933 1e−69 93 1267 182 700838329H1 SOYMON020 g2257597 BLASTN 935 1e−69 91 1268 182 700895548H1 SOYMON027 g2257597 BLASTN 916 1e−67 88 1269 182 700645519H1 SOYMON009 g2257597 BLASTN 904 1e−66 91 1270 182 701102605H1 SOYMON028 g2257597 BLASTN 882 1e−65 91 1271 182 701039360H1 SOYMON029 g2257597 BLASTN 546 1e−64 87 1272 182 701151305H1 SOYMON031 g2257597 BLASTN 661 1e−53 93 1273 182 701151405H1 SOYMON031 g2257597 BLASTN 696 1e−49 93 1274 182 700940911H1 SOYMON024 g2257597 BLASTN 356 1e−38 72 1275 182 700648994H1 SOYMON003 g2257597 BLASTN 529 1e−35 85 1276 182 700564729H1 SOYMON002 g2257597 BLASTN 451 1e−28 84 1277 23349 700894074H1 SOYMON024 g143760 BLASTX 137 1e−13 83 1278 5614 700558488H1 SOYMON001 g1161599 BLASTN 949 1e−70 84 1279 5614 700792287H1 SOYMON011 g1161599 BLASTN 935 1e−69 84 1280 5614 701000168H1 SOYMON018 g1161599 BLASTN 916 1e−67 81 1281 5614 700739376H1 SOYMON012 g1161599 BLASTN 920 1e−67 85 1282 5614 700854915H1 SOYMON023 g1161599 BLASTN 894 1e−65 87 1283 5614 700874304H1 SOYMON018 g1161599 BLASTN 827 1e−60 82 1284 5614 700656867H1 SOYMON004 g1161599 BLASTN 626 1e−43 84 1285 5614 700996544H1 SOYMON018 g1161599 BLASTN 385 1e−40 75 1286 5614 700742706H1 SOYMON012 g1161600 BLASTX 160 1e−15 88 1287 -GM16843 LIB3055-001- LIB3055 g1022802 BLASTN 665 1e−48 71 Q1-B1-B7 1288 -GM3918 LIB3029-012- LIB3029 g21834 BLASTN 241 1e−8 66 Q1-B1-G1 1289 16 LIB3040-022- LIB3040 g1161601 BLASTN 1074 1e−78 72 Q1-E1-D5 1290 16 LIB3039-049- LIB3039 g1161601 BLASTN 906 1e−66 75 Q1-E1-D8 1291 16 LIB3052-002- LIB3052 g1161601 BLASTN 858 1e−62 75 Q1-B1-H2 1292 16 LIB3040-020- LIB3040 g1161601 BLASTN 842 1e−61 75 Q1-E1-C8 1293 16 LIB3056-007- LIB3056 g1161601 BLASTN 849 1e−61 75 Q1-N1-G5 1294 16 LIB3039-040- LIB3039 g1161601 BLASTN 767 1e−55 74 Q1-E1-D8 1295 16 LIB3040-033- LIB3040 g1161601 BLASTN 418 1e−47 75 Q1-E1-B5 1296 16 LIB3039-012- LIB3039 g1161601 BLASTN 643 1e−42 74 Q1-E1-F12 1297 16 LIB3053-014- LIB3053 g1161602 BLASTX 101 1e−39 58 Q1-N1-A3 1298 1699 LIB3028-001- LIB3028 g21271 BLASTN 1151 1e−87 78 Q1-B1-A12 1299 1699 LIB3065-008- LIB3065 g21832 BLASTN 606 1e−40 79 Q1-N1-F5 1300 1699 LIB3055-012- LIB3055 g21832 BLASTN 457 1e−26 83 Q1-N1-E3 1301 1699 LIB3055-005- LIB3055 g21832 BLASTN 263 1e−13 76 Q1-N1-A2 1302 182 LIB3051-039- LIB3051 g2257597 BLASTN 1757 1e−140 90 Q1-K1-B6 1303 182 LIB3054-007- LIB3054 g2257597 BLASTN 1354 1e−112 88 Q1-N1-A7 1304 182 LIB3039-027- LIB3039 g2257597 BLASTN 1089 1e−110 90 Q1-E1-H9 1305 5614 LIB3049-026- LIB3049 g1161599 BLASTN 798 1e−88 84 Q1-E1-D8 1306 5614 LIB3028-006- LIB3028 g1161599 BLASTN 935 1e−69 86 Q1-B1-C12 1307 5614 LIB3028-007- LIB3028 g1161599 BLASTN 665 1e−44 83 Q1-B1-C11 MAIZE GLYCERALDEHYDE 3-PHOSPHATE DEHYDROGENASE 1308 -700016883 700016883H1 SATMON001 g1185553 BLASTN 459 1e−35 95 1309 -700021845 700021845H1 SATMON001 g1185553 BLASTN 379 1e−22 95 1310 -700042428 700042428H1 SATMON004 g168520 BLASTN 810 1e−61 87 1311 -700042586 700042586H1 SATMON004 g168478 BLASTN 572 1e−68 96 1312 -700076627 700076627H1 SATMON007 g1185553 BLASTN 406 1e−23 89 1313 -700082565 700082565H1 SATMON011 g1185553 BLASTN 415 1e−23 78 1314 -700083976 700083976H1 SATMON011 g22237 BLASTN 365 1e−21 90 1315 -700085105 700085105H1 SATMON011 g1185553 BLASTN 344 1e−17 74 1316 -700087058 700087058H1 SATMON011 g1184773 BLASTN 278 1e−14 98 1317 -700087967 700087967H1 SATMON011 g168478 BLASTN 1240 1e−94 100 1318 -700095618 700095618H1 SATMON008 g168478 BLASTN 567 1e−84 89 1319 -700098365 700098365H1 SATMON009 g168478 BLASTN 222 1e−9 80 1320 -700100580 700100580H1 SATMON009 g168478 BLASTN 463 1e−54 96 1321 -700103906 700103906H1 SATMON010 g1185553 BLASTN 329 1e−32 86 1322 -700152882 700152882H1 SATMON007 g293886 BLASTN 578 1e−39 94 1323 -700155165 700155165H1 SATMON007 g1184771 BLASTN 450 1e−28 100 1324 -700157523 700157523H1 SATMON012 g1185553 BLASTN 337 1e−17 97 1325 -700163947 700163947H1 SATMON013 g717080 BLASTN 327 1e−16 82 1326 -700197939 700197939H1 SATMON016 g22237 BLASTN 635 1e−44 82 1327 -700201904 700201904H1 SATMON003 g1185553 BLASTN 397 1e−22 88 1328 -700204190 700204190H1 SATMON003 g22302 BLASTN 295 1e−43 90 1329 -700236061 700236061H1 SATMON010 g1185553 BLASTN 273 1e−12 79 1330 -700238253 700238253H1 SATMON010 g2143408 BLASTN 1099 1e−82 96 1331 -700256918 700256918H1 SATMON017 g474407 BLASTN 1367 1e−112 98 1332 -700259576 700259576H1 SATMON017 g717080 BLASTN 280 1e−48 81 1333 -700263524 700263524H1 SATMON017 g22302 BLASTN 547 1e−59 97 1334 -700281884 700281884H2 SATMON021 g717080 BLASTN 296 1e−14 65 1335 -700340490 700340490H1 SATMON020 g1185553 BLASTN 372 1e−22 88 1336 -700346430 700346430H1 SATMON021 g1185553 BLASTN 334 1e−20 85 1337 -700349202 700349202H1 SATMON023 g157476 BLASTX 126 1e−22 71 1338 -700349272 700349272H1 SATMON023 g1100222 BLASTN 466 1e−28 67 1339 -700356209 700356209H1 SATMON024 g1184773 BLASTN 325 1e−24 95 1340 -700377496 700377496H1 SATMON019 g1184773 BLASTN 549 1e−70 93 1341 -700404753 700404753H1 SATMON026 g168520 BLASTN 455 1e−29 88 1342 -700421516 700421516H1 SATMONN01 g717080 BLASTN 269 1e−17 83 1343 -700427941 700427941H1 SATMONN01 g717080 BLASTN 524 1e−34 68 1344 -700428888 700428888H1 SATMONN01 g22302 BLASTN 232 1e−10 70 1345 -700432127 700432127H1 SATMONN01 g168521 BLASTN 269 1e−21 97 1346 -700438281 700438281H1 SATMON026 g168478 BLASTN 283 1e−38 92 1347 -700551026 700551026H1 SATMON022 g1185553 BLASTN 243 1e−9 72 1348 -700553346 700553346H1 SATMON022 g717080 BLASTN 218 1e−12 80 1349 -700570760 700570760H1 SATMON030 g1184773 BLASTN 358 1e−21 76 1350 -700580159 700580159H1 SATMON031 g1185553 BLASTN 381 1e−22 76 1351 -700616468 700616468H1 SATMON033 g1100225 BLASTX 160 1e−15 85 1352 -700616996 700616996H1 SATMON033 g20732 BLASTN 468 1e−30 80 1353 -700618295 700618295H1 SATMON033 g1184773 BLASTN 307 1e−47 89 1354 -700622760 700622760H1 SATMON034 g1184771 BLASTN 358 1e−24 86 1355 -700799777 700799777H1 SATMON036 g12158 BLASTN 198 1e−14 76 1356 -700801109 700801109H1 SATMON036 g22302 BLASTN 978 1e−92 99 1357 -701161482 701161482H1 SATMONN04 g1185553 BLASTN 310 1e−26 91 1358 -701166637 701166637H1 SATMONN04 g1184771 BLASTN 398 1e−24 86 1359 -701169309 701169309H1 SATMONN05 g168478 BLASTN 303 1e−14 69 1360 -701182137 701182137H1 SATMONN06 g168478 BLASTN 235 1e−8 91 1361 -701186041 701186041H1 SATMONN06 g1185555 BLASTN 261 1e−12 67 1362 11871 700017162H1 SATMON001 g1185553 BLASTN 479 1e−34 88 1363 11871 700100796H1 SATMON009 g1185553 BLASTN 480 1e−31 87 1364 11926 700623916H1 SATMON034 g168478 BLASTN 255 1e−10 76 1365 11926 700623908H1 SATMON034 g168478 BLASTN 241 1e−9 75 1366 1334 700470437H1 SATMON025 g717080 BLASTN 312 1e−19 80 1367 1334 700578860H1 SATMON031 g717080 BLASTN 310 1e−14 83 1368 14664 700163212H1 SATMON013 g1100222 BLASTN 844 1e−61 80 1369 14664 700382256H1 SATMON024 g1100222 BLASTN 764 1e−54 81 1370 1692 700085317H1 SATMON011 g3059121 BLASTN 970 1e−72 79 1371 1692 700222942H1 SATMON011 g1100222 BLASTN 898 1e−66 81 1372 1692 700618371H1 SATMON033 g3059121 BLASTN 554 1e−65 78 1373 1692 700381022H1 SATMON023 g1100222 BLASTN 660 1e−48 76 1374 1692 700264023H1 SATMON017 g1100222 BLASTN 678 1e−47 84 1375 1692 700258875H1 SATMON017 g1100222 BLASTN 556 1e−44 80 1376 1692 700612308H1 SATMON033 g460978 BLASTN 442 1e−28 80 1377 1692 700552370H1 SATMON022 g624679 BLASTX 124 1e−22 69 1378 1692 700458135H1 SATMON029 g1100222 BLASTN 299 1e−20 83 1379 17968 700339973H1 SATMON020 g1184775 BLASTN 1235 1e−98 100 1380 17968 700800152H1 SATMON036 g1184775 BLASTN 625 1e−43 100 1381 18309 700381457H1 SATMON023 g3101 BLASTN 444 1e−28 72 1382 19858 700102991H1 SATMON010 g1100223 BLASTX 118 1e−9 69 1383 20203 700017766H1 SATMON001 g1185553 BLASTN 525 1e−37 91 1384 20203 700020155H1 SATMON001 g1185553 BLASTN 518 1e−36 90 1385 2148 700617018H1 SATMON033 g474407 BLASTN 960 1e−112 95 1386 2148 701166093H1 SATMONN04 g474407 BLASTN 1005 1e−80 96 1387 2148 700430939H1 SATMONN01 g474407 BLASTN 438 1e−46 91 1388 22918 701175483H1 SATMONN05 g1185553 BLASTN 492 1e−32 88 1389 22918 701176645H1 SATMONN05 g1185553 BLASTN 397 1e−23 81 1390 2468 700100660H1 SATMON009 g168478 BLASTN 1490 1e−115 100 1391 2468 700097261H1 SATMON009 g22239 BLASTN 1135 1e−114 100 1392 2468 700097360H1 SATMON009 g168478 BLASTN 1468 1e−113 99 1393 2468 700098573H1 SATMON009 g22239 BLASTN 1305 1e−100 100 1394 2468 700101255H1 SATMON009 g168478 BLASTN 840 1e−85 96 1395 2468 700580636H1 SATMON031 g22239 BLASTN 903 1e−74 95 1396 2468 700044915H1 SATMON004 g22239 BLASTN 870 1e−63 100 1397 27323 700166009H1 SATMON013 g474407 BLASTN 1166 1e−88 99 1398 27323 700075283H1 SATMON007 g474407 BLASTN 997 1e−74 99 1399 30327 700158422H1 SATMON012 g22302 BLASTN 339 1e−44 83 1400 31280 700470273H1 SATMON025 g1185553 BLASTN 160 1e−8 71 1401 32165 700212044H1 SATMON016 g474407 BLASTN 1468 1e−113 99 1402 325 700201678H1 SATMON003 g22237 BLASTN 1478 1e−132 99 1403 325 700618123H1 SATMON033 g1184775 BLASTN 1007 1e−130 99 1404 325 700091437H1 SATMON011 g1184771 BLASTN 1162 1e−129 97 1405 325 700096907H1 SATMON008 g1184771 BLASTN 1650 1e−128 100 1406 325 700090956H1 SATMON011 g22237 BLASTN 1635 1e−127 100 1407 325 700573711H1 SATMON030 g1184773 BLASTN 1624 1e−126 99 1408 325 700208421H1 SATMON016 g22237 BLASTN 1606 1e−125 99 1409 325 700573153H1 SATMON030 g1184771 BLASTN 1392 1e−124 97 1410 325 700106667H1 SATMON010 g1184771 BLASTN 1595 1e−124 100 1411 325 700266257H1 SATMON017 g1184771 BLASTN 1595 1e−124 100 1412 325 700082726H1 SATMON011 g1184771 BLASTN 1599 1e−124 99 1413 325 700092552H1 SATMON008 g1184771 BLASTN 1585 1e−123 100 1414 325 700075862H1 SATMON007 g1184773 BLASTN 1589 1e−123 99 1415 325 700621325H1 SATMON034 g1184771 BLASTN 1589 1e−123 99 1416 325 700282389H2 SATMON023 g1184771 BLASTN 1590 1e−123 100 1417 325 700082207H1 SATMON011 g1184773 BLASTN 1568 1e−122 99 1418 325 700103258H1 SATMON010 g1184771 BLASTN 1575 1e−122 98 1419 325 700331931H1 SATMON019 g1184771 BLASTN 1575 1e−122 100 1420 325 700575033H1 SATMON030 g22237 BLASTN 763 1e−121 95 1421 325 700073504H1 SATMON007 g1184771 BLASTN 1412 1e−121 97 1422 325 700573737H1 SATMON030 g1184771 BLASTN 1540 1e−121 94 1423 325 700077448H1 SATMON007 g1184775 BLASTN 1555 1e−121 100 1424 325 700082338H1 SATMON011 g1184771 BLASTN 1560 1e−121 100 1425 325 700575985H1 SATMON030 g1184771 BLASTN 1208 1e−120 96 1426 325 700091658H1 SATMON011 g1184771 BLASTN 1453 1e−120 99 1427 325 700259305H1 SATMON017 g22237 BLASTN 1476 1e−120 99 1428 325 700092013H1 SATMON008 g22237 BLASTN 1545 1e−120 100 1429 325 700104625H1 SATMON010 g1184771 BLASTN 1545 1e−120 100 1430 325 700082934H1 SATMON011 g22237 BLASTN 1546 1e−120 99 1431 325 700083987H1 SATMON011 g1184771 BLASTN 1548 1e−120 99 1432 325 700084648H1 SATMON011 g22237 BLASTN 1551 1e−120 99 1433 325 700095742H1 SATMON008 g22237 BLASTN 1552 1e−120 99 1434 325 700049963H1 SATMON003 g1184771 BLASTN 1554 1e−120 99 1435 325 700086285H1 SATMON011 g1184771 BLASTN 1555 1e−120 100 1436 325 700622187H1 SATMON034 g1184771 BLASTN 1555 1e−120 98 1437 325 700082208H1 SATMON011 g1184771 BLASTN 1076 1e−119 99 1438 325 700615142H1 SATMON033 g1184775 BLASTN 1141 1e−119 98 1439 325 700072750H1 SATMON007 g1184773 BLASTN 1538 1e−119 99 1440 325 700210619H1 SATMON016 g22237 BLASTN 1540 1e−119 100 1441 325 700083321H1 SATMON011 g1184771 BLASTN 1540 1e−119 100 1442 325 700090105H1 SATMON011 g1184771 BLASTN 1541 1e−119 99 1443 325 700049167H1 SATMON003 g1184771 BLASTN 1033 1e−118 97 1444 325 700074010H1 SATMON007 g1184773 BLASTN 1523 1e−118 98 1445 325 700101165H1 SATMON009 g22237 BLASTN 1524 1e−118 99 1446 325 700049769H1 SATMON003 g1184771 BLASTN 1525 1e−118 100 1447 325 700263267H1 SATMON017 g1184771 BLASTN 1510 1e−117 100 1448 325 700265580H1 SATMON017 g22237 BLASTN 1510 1e−117 100 1449 325 700266447H1 SATMON017 g22237 BLASTN 1513 1e−117 99 1450 325 700026705H1 SATMON003 g1184771 BLASTN 1515 1e−117 100 1451 325 700098736H1 SATMON009 g22237 BLASTN 1515 1e−117 100 1452 325 700106693H1 SATMON010 g1184775 BLASTN 1517 1e−117 99 1453 325 700086276H1 SATMON011 g22237 BLASTN 1364 1e−116 92 1454 325 700087952H1 SATMON011 g1184771 BLASTN 1381 1e−116 99 1455 325 700206583H1 SATMON003 g22237 BLASTN 1400 1e−116 98 1456 325 700088779H1 SATMON011 g22237 BLASTN 1497 1e−116 99 1457 325 700212176H1 SATMON016 g1184773 BLASTN 1499 1e−116 99 1458 325 700085815H1 SATMON011 g1184773 BLASTN 1500 1e−116 100 1459 325 700085668H1 SATMON011 g22237 BLASTN 1501 1e−116 99 1460 325 700106805H1 SATMON010 g1184771 BLASTN 1501 1e−116 99 1461 325 700103136H1 SATMON010 g1184773 BLASTN 1502 1e−116 99 1462 325 700089503H1 SATMON011 g22237 BLASTN 1507 1e−116 99 1463 325 700260534H2 SATMON017 g22237 BLASTN 792 1e−115 97 1464 325 700083056H1 SATMON011 g1184771 BLASTN 970 1e−115 100 1465 325 700211911H1 SATMON016 g1184771 BLASTN 1300 1e−115 100 1466 325 700343952H1 SATMON021 g22237 BLASTN 1485 1e−115 100 1467 325 700220468H1 SATMON011 g1184771 BLASTN 1485 1e−115 100 1468 325 700331968H1 SATMON019 g1184771 BLASTN 1485 1e−115 100 1469 325 700077160H1 SATMON007 g1184775 BLASTN 1487 1e−115 99 1470 325 700466212H1 SATMON025 g22237 BLASTN 1487 1e−115 98 1471 325 700085480H1 SATMON011 g1184771 BLASTN 1488 1e−115 99 1472 325 700097118H1 SATMON009 g1184773 BLASTN 1489 1e−115 97 1473 325 700267631H1 SATMON017 g22237 BLASTN 1491 1e−115 99 1474 325 700106452H1 SATMON010 g1184771 BLASTN 1492 1e−115 98 1475 325 700349721H1 SATMON023 g1184775 BLASTN 1493 1e−115 99 1476 325 700084191H1 SATMON011 g1184773 BLASTN 1494 1e−115 99 1477 325 700265560H1 SATMON017 g22237 BLASTN 1495 1e−115 100 1478 325 700083729H1 SATMON011 g22237 BLASTN 1495 1e−115 100 1479 325 700074701H1 SATMON007 g1184773 BLASTN 779 1e−114 97 1480 325 700620211H1 SATMON034 g1184771 BLASTN 1149 1e−114 99 1481 325 700026713H1 SATMON003 g22237 BLASTN 1210 1e−114 100 1482 325 700102767H1 SATMON010 g1184773 BLASTN 1256 1e−114 98 1483 325 700048868H1 SATMON003 g1184773 BLASTN 1328 1e−114 99 1484 325 700211328H1 SATMON016 g1184771 BLASTN 1332 1e−114 97 1485 325 700348453H1 SATMON023 g22237 BLASTN 1473 1e−114 99 1486 325 700622770H1 SATMON034 g1184771 BLASTN 1474 1e−114 99 1487 325 700213013H1 SATMON016 g1184773 BLASTN 1479 1e−114 97 1488 325 700093628H1 SATMON008 g22237 BLASTN 1480 1e−114 100 1489 325 700201306H1 SATMON003 g1184775 BLASTN 1480 1e−114 100 1490 325 700083087H1 SATMON011 g22237 BLASTN 1480 1e−114 100 1491 325 700085692H1 SATMON011 g1184773 BLASTN 1481 1e−114 99 1492 325 700263282H1 SATMON017 g22237 BLASTN 1481 1e−114 99 1493 325 700049783H1 SATMON003 g1184773 BLASTN 1133 1e−113 99 1494 325 700446715H1 SATMON027 g22237 BLASTN 1228 1e−113 99 1495 325 700077235H1 SATMON007 g1184773 BLASTN 1460 1e−113 100 1496 325 700028530H1 SATMON003 g1184771 BLASTN 1460 1e−113 100 1497 325 700048175H1 SATMON003 g1184773 BLASTN 1460 1e−113 98 1498 325 700343356H1 SATMON021 g1184773 BLASTN 1464 1e−113 99 1499 325 700073041H1 SATMON007 g1184773 BLASTN 1465 1e−113 100 1500 325 700092544H1 SATMON008 g1184773 BLASTN 1466 1e−113 99 1501 325 700086852H1 SATMON011 g1184773 BLASTN 1470 1e−113 100 1502 325 700357153H1 SATMON024 g1184775 BLASTN 785 1e−112 99 1503 325 700576167H1 SATMON030 g1184771 BLASTN 1151 1e−112 96 1504 325 700262594H1 SATMON017 g22237 BLASTN 1241 1e−112 99 1505 325 700553438H1 SATMON022 g22237 BLASTN 1450 1e−112 100 1506 325 700053639H1 SATMON010 g22237 BLASTN 1450 1e−112 100 1507 325 700093171H1 SATMON008 g1184771 BLASTN 1451 1e−112 99 1508 325 700257051H1 SATMON017 g22237 BLASTN 1451 1e−112 97 1509 325 700106505H1 SATMON010 g1184771 BLASTN 1452 1e−112 99 1510 325 700104544H1 SATMON010 g1184773 BLASTN 1452 1e−112 98 1511 325 700072406H2 SATMON007 g1184771 BLASTN 1455 1e−112 100 1512 325 700048728H1 SATMON003 g1184773 BLASTN 1456 1e−112 98 1513 325 700076367H1 SATMON007 g1184771 BLASTN 1456 1e−112 99 1514 325 700381774H1 SATMON023 g22237 BLASTN 1458 1e−112 95 1515 325 700347358H1 SATMON021 g1184771 BLASTN 1036 1e−111 99 1516 325 700049511H1 SATMON003 g1184771 BLASTN 1051 1e−111 99 1517 325 700075705H1 SATMON007 g22237 BLASTN 1066 1e−111 99 1518 325 700047687H1 SATMON003 g1184771 BLASTN 1191 1e−111 99 1519 325 700206516H1 SATMON003 g1184773 BLASTN 1209 1e−111 97 1520 325 700210478H1 SATMON016 g1184771 BLASTN 1351 1e−111 99 1521 325 700087443H1 SATMON011 g1184771 BLASTN 1390 1e−111 97 1522 325 700103213H1 SATMON010 g1184771 BLASTN 1440 1e−111 100 1523 325 700071776H1 SATMON007 g22237 BLASTN 1442 1e−111 99 1524 325 700073331H1 SATMON007 g1184771 BLASTN 1444 1e−111 99 1525 325 700212530H1 SATMON016 g1184771 BLASTN 1446 1e−111 99 1526 325 700346220H1 SATMON021 g1184775 BLASTN 962 1e−110 98 1527 325 700346201H1 SATMON021 g22237 BLASTN 1089 1e−110 99 1528 325 700434507H1 SATMONN01 g22302 BLASTN 1375 1e−110 100 1529 325 700077047H1 SATMON007 g1184771 BLASTN 1425 1e−110 98 1530 325 700028536H1 SATMON003 g1184771 BLASTN 1425 1e−110 100 1531 325 700096704H1 SATMON008 g1184771 BLASTN 1425 1e−110 100 1532 325 700263591H1 SATMON017 g1184771 BLASTN 1426 1e−110 99 1533 325 700219528H1 SATMON011 g22237 BLASTN 1426 1e−110 99 1534 325 700094978H1 SATMON008 g22237 BLASTN 1431 1e−110 99 1535 325 700549520H1 SATMON022 g22237 BLASTN 1432 1e−110 99 1536 325 700082071H1 SATMON011 g1184773 BLASTN 1434 1e−110 99 1537 325 700092419H1 SATMON008 g1184773 BLASTN 1434 1e−110 93 1538 325 700347660H1 SATMON023 g1184771 BLASTN 1435 1e−110 100 1539 325 700100257H1 SATMON009 g1184771 BLASTN 1048 1e−109 96 1540 325 700381813H1 SATMON023 g22237 BLASTN 1090 1e−109 99 1541 325 700095790H1 SATMON008 g22237 BLASTN 1412 1e−109 99 1542 325 700342267H1 SATMON021 g1184773 BLASTN 1415 1e−109 98 1543 325 700349135H1 SATMON023 g1184771 BLASTN 1416 1e−109 99 1544 325 700344742H1 SATMON021 g22237 BLASTN 1423 1e−109 98 1545 325 700027120H1 SATMON003 g1184775 BLASTN 777 1e−108 99 1546 325 700029549H1 SATMON003 g1184771 BLASTN 1178 1e−108 99 1547 325 700051917H1 SATMON003 g1184775 BLASTN 1349 1e−108 97 1548 325 700053569H1 SATMON010 g22237 BLASTN 1401 1e−108 99 1549 325 700105941H1 SATMON010 g22237 BLASTN 1405 1e−108 100 1550 325 700219201H1 SATMON011 g22237 BLASTN 1406 1e−108 99 1551 325 700050951H1 SATMON003 g1184771 BLASTN 1406 1e−108 99 1552 325 700258792H1 SATMON017 g22237 BLASTN 1411 1e−108 97 1553 325 700084946H1 SATMON011 g22237 BLASTN 793 1e−107 99 1554 325 700571888H1 SATMON030 g1184775 BLASTN 1146 1e−107 96 1555 325 700029725H1 SATMON003 g1184771 BLASTN 1390 1e−107 100 1556 325 700802139H1 SATMON036 g1184773 BLASTN 1391 1e−107 99 1557 325 700030653H1 SATMON003 g22237 BLASTN 1395 1e−107 100 1558 325 700217462H1 SATMON016 g1184771 BLASTN 1395 1e−107 100 1559 325 700382314H1 SATMON024 g1184773 BLASTN 1396 1e−107 99 1560 325 700263059H1 SATMON017 g22237 BLASTN 1342 1e−106 98 1561 325 700332495H1 SATMON019 g1184773 BLASTN 1378 1e−106 98 1562 325 700053881H1 SATMON011 g1184773 BLASTN 1379 1e−106 97 1563 325 700216184H1 SATMON016 g22237 BLASTN 1385 1e−106 100 1564 325 700442583H1 SATMON026 g22237 BLASTN 1385 1e−106 100 1565 325 700089492H1 SATMON011 g1184771 BLASTN 1385 1e−106 100 1566 325 700211930H1 SATMON016 g1184773 BLASTN 1385 1e−106 97 1567 325 700262445H1 SATMON017 g22237 BLASTN 1386 1e−106 99 1568 325 700074068H1 SATMON007 g1184773 BLASTN 1387 1e−106 98 1569 325 700444054H1 SATMON027 g1184771 BLASTN 1387 1e−106 98 1570 325 700207212H1 SATMON017 g1184771 BLASTN 700 1e−105 97 1571 325 700349424H1 SATMON023 g1184773 BLASTN 723 1e−105 96 1572 325 700348215H1 SATMON023 g1184771 BLASTN 990 1e−105 96 1573 325 700345971H1 SATMON021 g1184773 BLASTN 1090 1e−105 98 1574 325 700048167H1 SATMON003 g1184771 BLASTN 1116 1e−105 98 1575 325 700081996H1 SATMON011 g1184771 BLASTN 1143 1e−105 96 1576 325 700104353H1 SATMON010 g1184771 BLASTN 1158 1e−105 96 1577 325 700026169H1 SATMON003 g1184771 BLASTN 1365 1e−105 100 1578 325 700405492H1 SATMON029 g1184771 BLASTN 1366 1e−105 99 1579 325 700354644H1 SATMON024 g1184773 BLASTN 1370 1e−105 100 1580 325 700442572H1 SATMON026 g1184771 BLASTN 1370 1e−105 100 1581 325 700612003H1 SATMON022 g22237 BLASTN 1370 1e−105 100 1582 325 700082158H1 SATMON011 g22237 BLASTN 1371 1e−105 99 1583 325 700348605H1 SATMON023 g1184771 BLASTN 1373 1e−105 98 1584 325 700045650H1 SATMON004 g22237 BLASTN 1375 1e−105 100 1585 325 700053842H1 SATMON011 g1184773 BLASTN 1375 1e−105 98 1586 325 700083488H1 SATMON011 g1184771 BLASTN 1375 1e−105 100 1587 325 700344378H1 SATMON021 g1184771 BLASTN 1040 1e−104 99 1588 325 700102971H1 SATMON010 g1184771 BLASTN 1143 1e−104 96 1589 325 700347294H1 SATMON021 g1184771 BLASTN 1177 1e−104 99 1590 325 700236512H1 SATMON010 g1184773 BLASTN 1205 1e−104 99 1591 325 700550622H1 SATMON022 g1184773 BLASTN 1311 1e−104 98 1592 325 700550613H1 SATMON022 g1184773 BLASTN 1322 1e−104 99 1593 325 700241417H1 SATMON010 g1184775 BLASTN 1353 1e−104 99 1594 325 700050635H1 SATMON003 g1184771 BLASTN 1354 1e−104 93 1595 325 700045260H1 SATMON004 g1184771 BLASTN 1355 1e−104 100 1596 325 700343844H1 SATMON021 g1184771 BLASTN 1355 1e−104 100 1597 325 700347975H1 SATMON023 g22237 BLASTN 1357 1e−104 98 1598 325 700345348H1 SATMON021 g1184773 BLASTN 1360 1e−104 100 1599 325 700345878H1 SATMON021 g22237 BLASTN 1360 1e−104 98 1600 325 700469928H1 SATMON025 g1184771 BLASTN 1361 1e−104 99 1601 325 700093631H1 SATMON008 g1184773 BLASTN 961 1e−103 99 1602 325 700427662H1 SATMONN01 g22302 BLASTN 1088 1e−103 99 1603 325 700099528H1 SATMON009 g1184771 BLASTN 1133 1e−103 96 1604 325 700347950H1 SATMON023 g1184773 BLASTN 1138 1e−103 98 1605 325 700267976H1 SATMON017 g1184771 BLASTN 1231 1e−103 96 1606 325 700224847H1 SATMON011 g22237 BLASTN 1255 1e−103 100 1607 325 700465854H1 SATMON025 g1184773 BLASTN 1294 1e−103 99 1608 325 700257309H1 SATMON017 g1184771 BLASTN 1302 1e−103 97 1609 325 700577862H1 SATMON031 g22237 BLASTN 1341 1e−103 99 1610 325 700550007H1 SATMON022 g1184773 BLASTN 1341 1e−103 99 1611 325 700573448H2 SATMON030 g1184771 BLASTN 1342 1e−103 99 1612 325 700217477H1 SATMON016 g1184771 BLASTN 1345 1e−103 100 1613 325 700381851H1 SATMON023 g1184771 BLASTN 734 1e−102 92 1614 325 700095091H1 SATMON008 g1184771 BLASTN 1112 1e−102 97 1615 325 700444008H1 SATMON027 g1184771 BLASTN 1123 1e−102 98 1616 325 700470785H1 SATMON025 g22237 BLASTN 1142 1e−102 98 1617 325 700551739H1 SATMON022 g22237 BLASTN 1245 1e−102 100 1618 325 700237938H1 SATMON010 g1184771 BLASTN 1292 1e−102 97 1619 325 700215507H1 SATMON016 g22237 BLASTN 1330 1e−102 98 1620 325 700350778H1 SATMON023 g1184771 BLASTN 1330 1e−102 98 1621 325 700029783H1 SATMON003 g22237 BLASTN 1330 1e−102 98 1622 325 701161421H1 SATMONN04 g1184771 BLASTN 1330 1e−102 100 1623 325 700209510H1 SATMON016 g22237 BLASTN 1331 1e−102 99 1624 325 700552375H1 SATMON022 g1184771 BLASTN 1332 1e−102 99 1625 325 701183327H1 SATMONN06 g1184771 BLASTN 1333 1e−102 98 1626 325 700611372H1 SATMON022 g22237 BLASTN 1335 1e−102 100 1627 325 700243589H1 SATMON010 g1184771 BLASTN 1335 1e−102 100 1628 325 700805727H1 SATMON036 g1184773 BLASTN 1339 1e−102 99 1629 325 700051631H1 SATMON003 g1184771 BLASTN 1339 1e−102 97 1630 325 700465454H1 SATMON025 g1184773 BLASTN 780 1e−101 100 1631 325 700348239H1 SATMON023 g1184773 BLASTN 989 1e−101 98 1632 325 700353680H1 SATMON024 g1184773 BLASTN 1171 1e−101 99 1633 325 700265106H1 SATMON017 g1184773 BLASTN 1292 1e−101 95 1634 325 700053220H1 SATMON008 g1184775 BLASTN 1317 1e−101 99 1635 325 700052903H1 SATMON007 g1184771 BLASTN 1317 1e−101 99 1636 325 700053069H1 SATMON007 g1184773 BLASTN 1319 1e−101 97 1637 325 700352222H1 SATMON023 g1184773 BLASTN 1322 1e−101 94 1638 325 700458334H1 SATMON029 g1184773 BLASTN 1323 1e−101 99 1639 325 700072219H1 SATMON007 g1184773 BLASTN 1323 1e−101 97 1640 325 700082679H1 SATMON011 g22237 BLASTN 1326 1e−101 99 1641 325 700219959H1 SATMON011 g1184775 BLASTN 1327 1e−101 99 1642 325 700216192H1 SATMON016 g1184771 BLASTN 1327 1e−101 99 1643 325 700453649H1 SATMON028 g1184771 BLASTN 1328 1e−101 99 1644 325 700611371H1 SATMON022 g22237 BLASTN 1328 1e−101 99 1645 325 700261174H1 SATMON017 g1184771 BLASTN 706 1e−100 95 1646 325 700378143H1 SATMON019 g1184771 BLASTN 1032 1e−100 95 1647 325 700345693H1 SATMON021 g1184773 BLASTN 1108 1e−100 98 1648 325 700075095H1 SATMON007 g1184773 BLASTN 1113 1e−100 99 1649 325 700549026H1 SATMON022 g1184771 BLASTN 1187 1e−100 98 1650 325 700333933H1 SATMON019 g22237 BLASTN 1228 1e−100 99 1651 325 700027389H1 SATMON003 g1184773 BLASTN 1305 1e−100 98 1652 325 700798802H1 SATMON036 g1184773 BLASTN 1306 1e−100 99 1653 325 700045878H1 SATMON004 g22237 BLASTN 1310 1e−100 98 1654 325 700087030H1 SATMON011 g1184773 BLASTN 1311 1e−100 94 1655 325 700221038H1 SATMON011 g1184771 BLASTN 1311 1e−100 99 1656 325 700333822H1 SATMON019 g1184771 BLASTN 1311 1e−100 93 1657 325 700085206H1 SATMON011 g1184773 BLASTN 1311 1e−100 99 1658 325 700161303H1 SATMON012 g1184775 BLASTN 1313 1e−100 98 1659 325 700087502H1 SATMON011 g1184771 BLASTN 1313 1e−100 98 1660 325 700105477H1 SATMON010 g1184773 BLASTN 1314 1e−100 99 1661 325 700441823H1 SATMON026 g1184771 BLASTN 1315 1e−100 100 1662 325 700196854H1 SATMON014 g1184771 BLASTN 1315 1e−100 100 1663 325 700457283H1 SATMON029 g1184771 BLASTN 1315 1e−100 100 1664 325 700223356H1 SATMON011 g1184773 BLASTN 1316 1e−100 99 1665 325 700550323H1 SATMON022 g1184771 BLASTN 1316 1e−100 99 1666 325 700212296H1 SATMON016 g1184771 BLASTN 895 1e−99 100 1667 325 700073907H1 SATMON007 g1184771 BLASTN 1154 1e−99 95 1668 325 700550683H1 SATMON022 g1184771 BLASTN 1266 1e−99 99 1669 325 700041553H1 SATMON004 g22302 BLASTN 1286 1e−99 97 1670 325 700197418H1 SATMON014 g1184775 BLASTN 1292 1e−99 99 1671 325 700083704H1 SATMON011 g22237 BLASTN 1293 1e−99 98 1672 325 700218362H1 SATMON016 g1184771 BLASTN 1295 1e−99 100 1673 325 700082314H1 SATMON011 g1184773 BLASTN 1295 1e−99 93 1674 325 700045668H1 SATMON004 g1184771 BLASTN 1297 1e−99 99 1675 325 700158619H1 SATMON012 g1184771 BLASTN 1297 1e−99 98 1676 325 700611967H1 SATMON022 g1184773 BLASTN 1298 1e−99 99 1677 325 700336112H1 SATMON019 g22237 BLASTN 1299 1e−99 98 1678 325 700444055H1 SATMON027 g1184771 BLASTN 1300 1e−99 100 1679 325 700236678H1 SATMON010 g1184771 BLASTN 1300 1e−99 100 1680 325 700214048H1 SATMON016 g1184773 BLASTN 1303 1e−99 99 1681 325 700351262H1 SATMON023 g1184773 BLASTN 1304 1e−99 94 1682 325 700583372H1 SATMON031 g1184771 BLASTN 632 1e−98 95 1683 325 700339709H1 SATMON020 g22237 BLASTN 852 1e−98 94 1684 325 700211842H1 SATMON016 g22237 BLASTN 920 1e−98 94 1685 325 700355436H1 SATMON024 g1184771 BLASTN 953 1e−98 98 1686 325 700221763H1 SATMON011 g22237 BLASTN 1011 1e−98 99 1687 325 700619245H1 SATMON034 g1184771 BLASTN 1012 1e−98 95 1688 325 700262781H1 SATMON017 g1184771 BLASTN 1016 1e−98 98 1689 325 700243153H1 SATMON010 g22237 BLASTN 1065 1e−98 100 1690 325 700344173H1 SATMON021 g1184771 BLASTN 1137 1e−98 97 1691 325 700349565H1 SATMON023 g1184771 BLASTN 1145 1e−98 96 1692 325 700157320H1 SATMON012 g1184773 BLASTN 1281 1e−98 99 1693 325 700611471H1 SATMON022 g22237 BLASTN 1282 1e−98 98 1694 325 700550503H1 SATMON022 g1184771 BLASTN 1283 1e−98 99 1695 325 700222893H1 SATMON011 g22237 BLASTN 1285 1e−98 100 1696 325 700242404H1 SATMON010 g1184771 BLASTN 1285 1e−98 100 1697 325 700218820H1 SATMON011 g1184771 BLASTN 1285 1e−98 100 1698 325 700220021H1 SATMON011 g22237 BLASTN 1286 1e−98 99 1699 325 700243542H1 SATMON010 g1184773 BLASTN 1286 1e−98 99 1700 325 700354379H1 SATMON024 g1184771 BLASTN 1288 1e−98 93 1701 325 700799328H1 SATMON036 g1184773 BLASTN 1289 1e−98 99 1702 325 700452454H1 SATMON028 g1184771 BLASTN 1290 1e−98 100 1703 325 700085246H1 SATMON011 g1184771 BLASTN 1290 1e−98 100 1704 325 700218590H1 SATMON011 g1184771 BLASTN 1290 1e−98 100 1705 325 700456377H1 SATMON029 g1184771 BLASTN 1291 1e−98 99 1706 325 700050750H1 SATMON003 g1185553 BLASTN 559 1e−97 99 1707 325 700351952H1 SATMON023 g1184771 BLASTN 797 1e−97 97 1708 325 700345594H1 SATMON021 g1184773 BLASTN 851 1e−97 99 1709 325 700267853H1 SATMON017 g1184771 BLASTN 890 1e−97 94 1710 325 700350105H1 SATMON023 g1184773 BLASTN 1006 1e−97 99 1711 325 700334557H1 SATMON019 g1184773 BLASTN 1028 1e−97 95 1712 325 700457542H1 SATMON029 g1184773 BLASTN 1067 1e−97 99 1713 325 700352772H1 SATMON024 g22237 BLASTN 1181 1e−97 98 1714 325 700550657H1 SATMON022 g22237 BLASTN 1226 1e−97 99 1715 325 700224772H1 SATMON011 g1184771 BLASTN 1270 1e−97 100 1716 325 700618874H1 SATMON034 g1184775 BLASTN 1270 1e−97 100 1717 325 700162968H1 SATMON013 g22237 BLASTN 1270 1e−97 100 1718 325 700025839H1 SATMON003 g1184775 BLASTN 1270 1e−97 100 1719 325 700075210H1 SATMON007 g1184773 BLASTN 1272 1e−97 93 1720 325 700025602H1 SATMON004 g22237 BLASTN 1275 1e−97 98 1721 325 700573453H2 SATMON030 g1184771 BLASTN 1276 1e−97 99 1722 325 700268153H1 SATMON017 g1184773 BLASTN 1277 1e−97 94 1723 325 700085062H1 SATMON011 g1184773 BLASTN 1279 1e−97 99 1724 325 700197210H1 SATMON014 g1184773 BLASTN 1280 1e−97 98 1725 325 700053187H1 SATMON008 g22237 BLASTN 1280 1e−97 100 1726 325 700239541H1 SATMON010 g1184771 BLASTN 1280 1e−97 100 1727 325 700381789H1 SATMON023 g1184773 BLASTN 1280 1e−97 93 1728 325 700382074H1 SATMON024 g1184773 BLASTN 737 1e−96 93 1729 325 700615886H1 SATMON033 g1184771 BLASTN 814 1e−96 96 1730 325 700203271H1 SATMON003 g1184771 BLASTN 1047 1e−96 96 1731 325 700090047H1 SATMON011 g1184771 BLASTN 1047 1e−96 96 1732 325 700345983H1 SATMON021 g1184771 BLASTN 1048 1e−96 96 1733 325 700580224H1 SATMON031 g1184771 BLASTN 1060 1e−96 94 1734 325 700163304H1 SATMON013 g1184771 BLASTN 1260 1e−96 100 1735 325 700218377H1 SATMON016 g1184771 BLASTN 1260 1e−96 100 1736 325 700090628H1 SATMON011 g22237 BLASTN 1262 1e−96 98 1737 325 700205936H1 SATMON003 g1184773 BLASTN 1265 1e−96 91 1738 325 700087928H1 SATMON011 g22237 BLASTN 1265 1e−96 100 1739 325 700195069H1 SATMON014 g1184775 BLASTN 1266 1e−96 98 1740 325 700552795H1 SATMON022 g1184773 BLASTN 658 1e−95 94 1741 325 700093666H1 SATMON008 g22237 BLASTN 873 1e−95 96 1742 325 700196963H1 SATMON014 g1184773 BLASTN 957 1e−95 98 1743 325 700083992H1 SATMON011 g1184773 BLASTN 1034 1e−95 96 1744 325 700334351H1 SATMON019 g1184773 BLASTN 1162 1e−95 96 1745 325 700165979H1 SATMON013 g22237 BLASTN 1211 1e−95 98 1746 325 700612175H1 SATMON022 g1184773 BLASTN 1245 1e−95 100 1747 325 700157886H1 SATMON012 g1184771 BLASTN 1245 1e−95 100 1748 325 700218843H1 SATMON011 g22237 BLASTN 1246 1e−95 99 1749 325 700223241H1 SATMON011 g22237 BLASTN 1253 1e−95 99 1750 325 700382157H1 SATMON024 g1184773 BLASTN 1254 1e−95 93 1751 325 700163655H1 SATMON013 g22237 BLASTN 1255 1e−95 100 1752 325 700219734H1 SATMON011 g1184773 BLASTN 1256 1e−95 99 1753 325 700258401H1 SATMON017 g22237 BLASTN 744 1e−94 91 1754 325 700569409H2 SATMON030 g1184771 BLASTN 755 1e−94 100 1755 325 700449985H1 SATMON028 g22237 BLASTN 1041 1e−94 99 1756 325 700209417H1 SATMON016 g22237 BLASTN 1192 1e−94 96 1757 325 700218233H1 SATMON016 g1184773 BLASTN 1235 1e−94 98 1758 325 700023172H1 SATMON003 g1184773 BLASTN 1241 1e−94 99 1759 325 700165002H1 SATMON013 g1184771 BLASTN 1242 1e−94 99 1760 325 700240575H1 SATMON010 g1184771 BLASTN 1243 1e−94 98 1761 325 700193127H1 SATMON014 g1184775 BLASTN 1243 1e−94 98 1762 325 700202138H1 SATMON003 g1184771 BLASTN 635 1e−93 94 1763 325 700619314H1 SATMON034 g1184771 BLASTN 697 1e−93 93 1764 325 700611272H1 SATMON022 g22237 BLASTN 743 1e−93 97 1765 325 700235577H1 SATMON010 g1184771 BLASTN 810 1e−93 98 1766 325 700048739H1 SATMON003 g1184771 BLASTN 1012 1e−93 97 1767 325 700337602H1 SATMON020 g22237 BLASTN 1097 1e−93 97 1768 325 700457423H1 SATMON029 g22237 BLASTN 1138 1e−93 98 1769 325 700048682H1 SATMON003 g1184773 BLASTN 1154 1e−93 92 1770 325 700456449H1 SATMON029 g1184773 BLASTN 1221 1e−93 94 1771 325 700239518H1 SATMON010 g1184771 BLASTN 1228 1e−93 98 1772 325 700457982H1 SATMON029 g22237 BLASTN 1229 1e−93 96 1773 325 700103576H1 SATMON010 g1184771 BLASTN 1230 1e−93 98 1774 325 700454265H1 SATMON029 g1184771 BLASTN 555 1e−92 96 1775 325 700340854H1 SATMON020 g22237 BLASTN 580 1e−92 97 1776 325 700458888H1 SATMON029 g1184771 BLASTN 769 1e−92 98 1777 325 700581403H1 SATMON031 g1184771 BLASTN 775 1e−92 96 1778 325 700224722H1 SATMON011 g22237 BLASTN 979 1e−92 94 1779 325 700217644H1 SATMON016 g1184771 BLASTN 1072 1e−92 96 1780 325 700454195H1 SATMON029 g22237 BLASTN 1084 1e−92 96 1781 325 700215504H1 SATMON016 g1184775 BLASTN 1122 1e−92 96 1782 325 700214190H1 SATMON016 g1184771 BLASTN 1210 1e−92 100 1783 325 700456941H1 SATMON029 g1184771 BLASTN 1211 1e−92 94 1784 325 700193816H1 SATMON014 g1184775 BLASTN 1212 1e−92 99 1785 325 700241930H1 SATMON010 g1184771 BLASTN 1213 1e−92 98 1786 325 700160162H1 SATMON012 g1184775 BLASTN 1215 1e−92 98 1787 325 700171289H1 SATMON013 g22237 BLASTN 1220 1e−92 100 1788 325 700549474H1 SATMON022 g1184773 BLASTN 665 1e−91 100 1789 325 700422573H1 SATMONN01 g22237 BLASTN 715 1e−91 92 1790 325 700377664H1 SATMON019 g1184771 BLASTN 747 1e−91 94 1791 325 700193034H1 SATMON014 g1184775 BLASTN 881 1e−91 99 1792 325 700163652H1 SATMON013 g1184771 BLASTN 990 1e−91 100 1793 325 700212649H1 SATMON016 g22237 BLASTN 1159 1e−91 99 1794 325 700165066H1 SATMON013 g1184771 BLASTN 1201 1e−91 99 1795 325 700152004H1 SATMON007 g1184773 BLASTN 1202 1e−91 99 1796 325 700243428H1 SATMON010 g1184773 BLASTN 1203 1e−91 99 1797 325 700167249H1 SATMON013 g1184771 BLASTN 1206 1e−91 99 1798 325 700150450H1 SATMON007 g1184773 BLASTN 1206 1e−91 99 1799 325 700089949H1 SATMON011 g1184771 BLASTN 599 1e−90 83 1800 325 700443495H1 SATMON027 g1184771 BLASTN 617 1e−90 97 1801 325 700469283H1 SATMON025 g1184771 BLASTN 672 1e−90 98 1802 325 700072276H1 SATMON007 g1184771 BLASTN 916 1e−90 96 1803 325 700457552H1 SATMON029 g1184771 BLASTN 953 1e−90 96 1804 325 700351671H1 SATMON023 g1184771 BLASTN 984 1e−90 99 1805 325 700571583H1 SATMON030 g22237 BLASTN 1059 1e−90 94 1806 325 700803969H1 SATMON036 g1184773 BLASTN 1186 1e−90 93 1807 325 700150936H1 SATMON007 g1184773 BLASTN 1196 1e−90 94 1808 325 700570929H1 SATMON030 g1184773 BLASTN 495 1e−89 100 1809 325 700338407H1 SATMON020 g1184773 BLASTN 1065 1e−89 95 1810 325 700021640H1 SATMON001 g1184771 BLASTN 1173 1e−89 99 1811 325 700151914H1 SATMON007 g1184773 BLASTN 1175 1e−89 100 1812 325 700167480H1 SATMON013 g22237 BLASTN 1176 1e−89 98 1813 325 700236453H1 SATMON010 g1184771 BLASTN 1178 1e−89 98 1814 325 700238168H1 SATMON010 g1184771 BLASTN 1182 1e−89 99 1815 325 700613413H1 SATMON033 g1184771 BLASTN 484 1e−88 91 1816 325 700357450H1 SATMON024 g1184773 BLASTN 527 1e−88 98 1817 325 700450090H2 SATMON028 g1184771 BLASTN 684 1e−88 93 1818 325 700801459H1 SATMON036 g1184773 BLASTN 850 1e−88 99 1819 325 700457313H1 SATMON029 g22237 BLASTN 855 1e−88 100 1820 325 700382823H1 SATMON024 g1184773 BLASTN 875 1e−88 96 1821 325 700085440H1 SATMON011 g1184771 BLASTN 951 1e−88 97 1822 325 700216971H1 SATMON016 g1184771 BLASTN 951 1e−88 97 1823 325 700239980H1 SATMON010 g1184771 BLASTN 1123 1e−88 98 1824 325 700801083H1 SATMON036 g1184773 BLASTN 1162 1e−88 93 1825 325 700202393H1 SATMON003 g1184775 BLASTN 1166 1e−88 98 1826 325 700105153H1 SATMON010 g1184771 BLASTN 1169 1e−88 99 1827 325 700087788H1 SATMON011 g1184771 BLASTN 1169 1e−88 96 1828 325 700152166H1 SATMON007 g22237 BLASTN 1171 1e−88 99 1829 325 700332968H1 SATMON019 g22237 BLASTN 437 1e−87 93 1830 325 700204350H1 SATMON003 g1184771 BLASTN 441 1e−87 96 1831 325 700150168H1 SATMON007 g1184773 BLASTN 901 1e−87 98 1832 325 700449984H1 SATMON028 g22237 BLASTN 907 1e−87 94 1833 325 700156642H1 SATMON012 g1184773 BLASTN 1149 1e−87 98 1834 325 700152779H1 SATMON007 g1184773 BLASTN 1150 1e−87 100 1835 325 700160261H1 SATMON012 g1184775 BLASTN 1151 1e−87 99 1836 325 700804718H1 SATMON036 g1184775 BLASTN 1153 1e−87 97 1837 325 700356233H1 SATMON024 g1184775 BLASTN 1156 1e−87 99 1838 325 700043272H1 SATMON004 g1184771 BLASTN 1160 1e−87 92 1839 325 700456666H1 SATMON029 g1184771 BLASTN 519 1e−86 94 1840 325 700205926H1 SATMON003 g1184771 BLASTN 587 1e−86 98 1841 325 700454102H1 SATMON029 g1184771 BLASTN 670 1e−86 94 1842 325 700207045H1 SATMON003 g1184771 BLASTN 935 1e−86 95 1843 325 700377244H1 SATMON019 g1184771 BLASTN 985 1e−86 99 1844 325 700549440H1 SATMON022 g1184773 BLASTN 990 1e−86 100 1845 325 700166882H1 SATMON013 g22237 BLASTN 1141 1e−86 97 1846 325 700167140H1 SATMON013 g1184771 BLASTN 1143 1e−86 97 1847 325 700152640H1 SATMON007 g1184773 BLASTN 1145 1e−86 100 1848 325 700020603H1 SATMON001 g22237 BLASTN 1146 1e−86 99 1849 325 700152109H1 SATMON007 g1184773 BLASTN 1147 1e−86 99 1850 325 700442690H1 SATMON026 g1184771 BLASTN 635 1e−85 95 1851 325 700156713H1 SATMON012 g1184775 BLASTN 705 1e−85 100 1852 325 700239313H1 SATMON010 g1184771 BLASTN 907 1e−85 92 1853 325 700102871H1 SATMON010 g1184771 BLASTN 916 1e−85 96 1854 325 700224872H1 SATMON011 g1184771 BLASTN 916 1e−85 96 1855 325 700448596H1 SATMON028 g1184771 BLASTN 951 1e−85 95 1856 325 700218841H1 SATMON011 g1184771 BLASTN 998 1e−85 93 1857 325 700258654H1 SATMON017 g1184771 BLASTN 1090 1e−85 97 1858 325 700798771H1 SATMON036 g1184771 BLASTN 1125 1e−85 100 1859 325 700152891H1 SATMON007 g22237 BLASTN 1126 1e−85 99 1860 325 700805450H1 SATMON036 g1184773 BLASTN 1130 1e−85 94 1861 325 700152783H1 SATMON007 g22237 BLASTN 1131 1e−85 99 1862 325 700085765H1 SATMON011 g1184771 BLASTN 1135 1e−85 100 1863 325 700263179H1 SATMON017 g22237 BLASTN 827 1e−84 99 1864 325 700163973H1 SATMON013 g22237 BLASTN 1113 1e−84 97 1865 325 700152630H1 SATMON007 g1184773 BLASTN 1115 1e−84 100 1866 325 700152546H1 SATMON007 g22237 BLASTN 1116 1e−84 99 1867 325 700217728H1 SATMON016 g1184773 BLASTN 1118 1e−84 99 1868 325 700336157H1 SATMON019 g1184773 BLASTN 1119 1e−84 91 1869 325 700332651H1 SATMON019 g1184775 BLASTN 908 1e−83 96 1870 325 700348702H1 SATMON023 g1184771 BLASTN 963 1e−83 87 1871 325 700611336H1 SATMON022 g22237 BLASTN 1042 1e−83 90 1872 325 700151934H1 SATMON007 g1184773 BLASTN 1105 1e−83 100 1873 325 700150270H1 SATMON007 g1184773 BLASTN 1106 1e−83 99 1874 325 700021115H1 SATMON001 g1184771 BLASTN 1111 1e−83 97 1875 325 700213761H1 SATMON016 g1184773 BLASTN 1111 1e−83 97 1876 325 700083759H1 SATMON011 g1184773 BLASTN 596 1e−82 93 1877 325 700263853H1 SATMON017 g1184771 BLASTN 883 1e−82 95 1878 325 700347719H1 SATMON023 g1184775 BLASTN 996 1e−82 96 1879 325 700048938H1 SATMON003 g1184775 BLASTN 1014 1e−82 97 1880 325 700150141H1 SATMON007 g1184771 BLASTN 1095 1e−82 100 1881 325 700019545H1 SATMON001 g1184773 BLASTN 1095 1e−82 100 1882 325 700019463H1 SATMON001 g1184773 BLASTN 1096 1e−82 97 1883 325 700455246H1 SATMON029 g1184771 BLASTN 1100 1e−82 92 1884 325 700382892H1 SATMON024 g1184773 BLASTN 613 1e−81 89 1885 325 700346309H1 SATMON021 g1184771 BLASTN 858 1e−81 92 1886 325 700257372H1 SATMON017 g1184771 BLASTN 903 1e−81 94 1887 325 700802008H1 SATMON036 g1184775 BLASTN 969 1e−81 97 1888 325 700083602H1 SATMON011 g22237 BLASTN 1081 1e−81 96 1889 325 700266939H1 SATMON017 g22237 BLASTN 1083 1e−81 98 1890 325 700431491H1 SATMONN01 g22237 BLASTN 1084 1e−81 87 1891 325 700611180H1 SATMON022 g22237 BLASTN 481 1e−80 91 1892 325 700348016H1 SATMON023 g1184773 BLASTN 611 1e−80 89 1893 325 700577294H1 SATMON031 g1184771 BLASTN 809 1e−80 92 1894 325 700457970H1 SATMON029 g1184771 BLASTN 934 1e−80 96 1895 325 700239677H1 SATMON010 g1184773 BLASTN 1066 1e−80 93 1896 325 700242889H1 SATMON010 g1184773 BLASTN 1066 1e−80 99 1897 325 700016313H1 SATMON001 g22237 BLASTN 1072 1e−80 99 1898 325 700155241H1 SATMON007 g1184771 BLASTN 1076 1e−80 99 1899 325 700223882H1 SATMON011 g1184771 BLASTN 696 1e−79 90 1900 325 700047915H1 SATMON003 g1184771 BLASTN 724 1e−79 98 1901 325 700449818H2 SATMON028 g1184771 BLASTN 761 1e−79 91 1902 325 700804993H1 SATMON036 g1184773 BLASTN 827 1e−79 98 1903 325 700570972H1 SATMON030 g1184773 BLASTN 867 1e−79 97 1904 325 700016664H1 SATMON001 g1185553 BLASTN 885 1e−79 100 1905 325 700213557H1 SATMON016 g1184773 BLASTN 908 1e−79 92 1906 325 700613214H1 SATMON033 g1184771 BLASTN 997 1e−79 88 1907 325 700343710H1 SATMON021 g1184773 BLASTN 1055 1e−79 88 1908 325 700442421H1 SATMON026 g22237 BLASTN 501 1e−78 96 1909 325 700265008H1 SATMON017 g1184773 BLASTN 866 1e−78 98 1910 325 700218525H1 SATMON011 g1184771 BLASTN 899 1e−78 96 1911 325 700551922H1 SATMON022 g22237 BLASTN 1045 1e−78 97 1912 325 700017612H1 SATMON001 g22237 BLASTN 1047 1e−78 96 1913 325 700579349H1 SATMON031 g22237 BLASTN 791 1e−77 87 1914 325 700197914H1 SATMON016 g1184771 BLASTN 811 1e−77 96 1915 325 700083456H1 SATMON011 g1184773 BLASTN 1035 1e−77 86 1916 325 700018387H1 SATMON001 g1184771 BLASTN 1035 1e−77 100 1917 325 700611470H1 SATMON022 g22237 BLASTN 618 1e−76 87 1918 325 700074067H1 SATMON007 g22237 BLASTN 837 1e−76 95 1919 325 700237659H1 SATMON010 g1184771 BLASTN 957 1e−76 96 1920 325 700018236H1 SATMON001 g1184773 BLASTN 1025 1e−76 100 1921 325 700240687H1 SATMON010 g1184771 BLASTN 957 1e−75 96 1922 325 700152594H1 SATMON007 g1184773 BLASTN 1009 1e−75 93 1923 325 700050944H1 SATMON003 g1184771 BLASTN 1009 1e−75 94 1924 325 700016175H1 SATMON001 g1184775 BLASTN 1015 1e−75 96 1925 325 700238172H1 SATMON010 g1184771 BLASTN 1016 1e−75 99 1926 325 700349862H1 SATMON023 g22237 BLASTN 459 1e−74 96 1927 325 700336123H1 SATMON019 g1184771 BLASTN 842 1e−74 89 1928 325 700151243H1 SATMON007 g22237 BLASTN 994 1e−74 99 1929 325 700164181H1 SATMON013 g1184773 BLASTN 998 1e−74 98 1930 325 700149684H1 SATMON007 g1184773 BLASTN 999 1e−74 93 1931 325 700615060H1 SATMON033 g1184773 BLASTN 469 1e−73 90 1932 325 700456658H1 SATMON029 g1184771 BLASTN 580 1e−73 93 1933 325 700151426H1 SATMON007 g1184771 BLASTN 618 1e−73 100 1934 325 700261414H1 SATMON017 g1184771 BLASTN 709 1e−73 95 1935 325 700353168H1 SATMON024 g1184773 BLASTN 716 1e−73 91 1936 325 700350156H1 SATMON023 g1184771 BLASTN 757 1e−73 88 1937 325 700171133H1 SATMON013 g1184771 BLASTN 771 1e−73 94 1938 325 700150636H1 SATMON007 g1184771 BLASTN 771 1e−73 96 1939 325 700354231H1 SATMON024 g1184773 BLASTN 984 1e−73 98 1940 325 700454489H1 SATMON029 g22237 BLASTN 565 1e−72 94 1941 325 700241567H1 SATMON010 g1184771 BLASTN 622 1e−72 94 1942 325 700171506H1 SATMON013 g22237 BLASTN 847 1e−72 98 1943 325 700354944H1 SATMON024 g1184773 BLASTN 974 1e−72 93 1944 325 700160388H1 SATMON012 g1184773 BLASTN 974 1e−72 93 1945 325 700806125H1 SATMON036 g1184773 BLASTN 976 1e−72 87 1946 325 700072347H2 SATMON007 g1184773 BLASTN 962 1e−71 92 1947 325 700264638H1 SATMON017 g1185553 BLASTN 568 1e−70 95 1948 325 701181725H1 SATMONN06 g1184773 BLASTN 796 1e−70 91 1949 325 700439643H1 SATMON026 g1184771 BLASTN 885 1e−70 89 1950 325 700473276H1 SATMON025 g1184771 BLASTN 953 1e−70 99 1951 325 700335504H1 SATMON019 g1184773 BLASTN 597 1e−69 82 1952 325 700439983H1 SATMON026 g1184771 BLASTN 810 1e−69 99 1953 325 700803685H1 SATMON036 g1184773 BLASTN 825 1e−69 94 1954 325 700089572H1 SATMON011 g1184773 BLASTN 943 1e−69 99 1955 325 700620191H1 SATMON034 g1184771 BLASTN 838 1e−68 90 1956 325 700336318H1 SATMON019 g22237 BLASTN 930 1e−68 100 1957 325 700218257H1 SATMON016 g22237 BLASTN 584 1e−67 88 1958 325 700471821H1 SATMON025 g1184771 BLASTN 590 1e−67 100 1959 325 700335407H1 SATMON019 g22237 BLASTN 912 1e−67 79 1960 325 700242905H1 SATMON010 g1184771 BLASTN 577 1e−66 93 1961 325 700333089H1 SATMON019 g1184773 BLASTN 760 1e−66 93 1962 325 700615210H1 SATMON033 g1184773 BLASTN 824 1e−66 93 1963 325 700197701H1 SATMON014 g1184773 BLASTN 901 1e−66 82 1964 325 700017877H1 SATMON001 g1184771 BLASTN 526 1e−64 93 1965 325 700467503H1 SATMON025 g293888 BLASTN 510 1e−63 94 1966 325 700457187H1 SATMON029 g1184771 BLASTN 648 1e−63 86 1967 325 700381477H1 SATMON023 g1184773 BLASTN 837 1e−63 98 1968 325 700614350H1 SATMON033 g22237 BLASTN 868 1e−63 96 1969 325 700092925H1 SATMON008 g22237 BLASTN 752 1e−62 94 1970 325 700016350H1 SATMON001 g22237 BLASTN 853 1e−62 98 1971 325 700019729H1 SATMON001 g22237 BLASTN 853 1e−62 98 1972 325 700167419H1 SATMON013 g1184771 BLASTN 860 1e−62 100 1973 325 700152703H1 SATMON007 g22237 BLASTN 860 1e−62 100 1974 325 700449337H1 SATMON028 g1184771 BLASTN 860 1e−62 100 1975 325 700151887H1 SATMON007 g1184775 BLASTN 848 1e−61 99 1976 325 700578028H1 SATMON031 g1184771 BLASTN 618 1e−60 91 1977 325 700440305H1 SATMON026 g1184771 BLASTN 660 1e−60 97 1978 325 700354945H1 SATMON024 g1184775 BLASTN 837 1e−60 98 1979 325 700341302H1 SATMON020 g1184771 BLASTN 375 1e−59 91 1980 325 700026117H1 SATMON003 g1185553 BLASTN 501 1e−58 98 1981 325 700150218H1 SATMON007 g1184771 BLASTN 732 1e−58 93 1982 325 700446832H1 SATMON027 g1184771 BLASTN 802 1e−58 97 1983 325 700171562H1 SATMON013 g1184771 BLASTN 805 1e−58 100 1984 325 700156216H1 SATMON007 g1184773 BLASTN 779 1e−56 87 1985 325 700095551H1 SATMON008 g22237 BLASTN 779 1e−56 98 1986 325 701165479H1 SATMONN04 g1184771 BLASTN 786 1e−56 98 1987 325 700151917H1 SATMON007 g1184773 BLASTN 682 1e−55 90 1988 325 700153313H1 SATMON007 g22237 BLASTN 771 1e−55 99 1989 325 700204963H1 SATMON003 g1184771 BLASTN 472 1e−54 93 1990 325 700450961H1 SATMON028 g22237 BLASTN 480 1e−54 99 1991 325 700434230H1 SATMONN01 g1184771 BLASTN 765 1e−54 93 1992 325 700265994H1 SATMON017 g22237 BLASTN 748 1e−53 88 1993 325 700090231H1 SATMON011 g1184773 BLASTN 750 1e−53 100 1994 325 700073935H1 SATMON007 g1184773 BLASTN 751 1e−53 99 1995 325 700084392H1 SATMON011 g22237 BLASTN 640 1e−52 100 1996 325 700382560H1 SATMON024 g1184773 BLASTN 730 1e−52 81 1997 325 700257449H2 SATMON017 g1184771 BLASTN 555 1e−51 97 1998 325 700210766H1 SATMON016 g22237 BLASTN 723 1e−51 99 1999 325 700427913H1 SATMONN01 g22237 BLASTN 728 1e−51 98 2000 325 700351216H1 SATMON023 g1184771 BLASTN 550 1e−50 98 2001 325 700806073H1 SATMON036 g1184773 BLASTN 390 1e−49 79 2002 325 700207249H1 SATMON017 g1184771 BLASTN 480 1e−49 95 2003 325 700261719H1 SATMON017 g1184771 BLASTN 611 1e−49 94 2004 325 700430989H1 SATMONN01 g22237 BLASTN 631 1e−49 90 2005 325 700807308H1 SATMON036 g1184773 BLASTN 698 1e−49 86 2006 325 700334327H1 SATMON019 g1184771 BLASTN 704 1e−49 97 2007 325 700172805H1 SATMON013 g1184771 BLASTN 705 1e−49 95 2008 325 700422633H1 SATMONN01 g1184771 BLASTN 411 1e−47 89 2009 325 700353962H1 SATMON024 g1184773 BLASTN 678 1e−47 99 2010 325 701161133H1 SATMONN04 g1184771 BLASTN 655 1e−45 100 2011 325 700802550H1 SATMON036 g1184773 BLASTN 438 1e−44 92 2012 325 700440239H1 SATMON026 g22237 BLASTN 449 1e−44 95 2013 325 700454565H1 SATMON029 g1184771 BLASTN 524 1e−44 89 2014 325 700053528H1 SATMON010 g22237 BLASTN 635 1e−44 100 2015 325 700257743H1 SATMON017 g1184771 BLASTN 352 1e−43 92 2016 325 700072283H1 SATMON007 g1184773 BLASTN 626 1e−43 99 2017 325 700260796H1 SATMON017 g22237 BLASTN 628 1e−43 99 2018 325 700262496H1 SATMON017 g1184771 BLASTN 455 1e−42 90 2019 325 700155358H1 SATMON007 g1184771 BLASTN 610 1e−42 100 2020 325 700196762H1 SATMON014 g1184773 BLASTN 615 1e−42 100 2021 325 700450601H1 SATMON028 g22237 BLASTN 615 1e−42 96 2022 325 700581050H1 SATMON031 g22237 BLASTN 618 1e−42 99 2023 325 700072316H2 SATMON007 g1184773 BLASTN 366 1e−40 92 2024 325 700427659H1 SATMONN01 g22302 BLASTN 416 1e−38 94 2025 325 700356507H1 SATMON024 g1184773 BLASTN 422 1e−38 89 2026 325 700169472H1 SATMON013 g1184773 BLASTN 339 1e−37 93 2027 325 700377362H1 SATMON019 g1184773 BLASTN 550 1e−37 97 2028 325 700378460H1 SATMON020 g1184771 BLASTN 345 1e−36 100 2029 325 700440218H1 SATMON026 g22237 BLASTN 538 1e−36 91 2030 325 700440230H1 SATMON026 g22237 BLASTN 364 1e−35 97 2031 325 700072350H1 SATMON007 g1184773 BLASTN 470 1e−35 99 2032 325 700241920H1 SATMON010 g22302 BLASTN 528 1e−35 99 2033 325 700347048H1 SATMON021 g1184773 BLASTN 537 1e−35 90 2034 325 700802555H1 SATMON036 g1184773 BLASTN 438 1e−34 88 2035 325 700615893H1 SATMON033 g1184773 BLASTN 372 1e−33 92 2036 325 700257073H1 SATMON017 g1184771 BLASTN 430 1e−32 90 2037 325 700220433H1 SATMON011 g1184773 BLASTN 490 1e−32 91 2038 325 700073453H1 SATMON007 g1184773 BLASTN 497 1e−32 92 2039 325 700086779H1 SATMON011 g1184771 BLASTN 480 1e−31 96 2040 325 700621224H1 SATMON034 g1184771 BLASTN 278 1e−30 98 2041 325 700344636H1 SATMON021 g22237 BLASTN 461 1e−29 98 2042 325 700240570H1 SATMON010 g1184771 BLASTN 463 1e−29 95 2043 325 700349592H1 SATMON023 g1184773 BLASTN 325 1e−28 90 2044 325 700454979H1 SATMON029 g22237 BLASTN 412 1e−25 92 2045 325 700206008H1 SATMON003 g22237 BLASTN 191 1e−23 99 2046 325 700263545H1 SATMON017 g22237 BLASTN 300 1e−23 95 2047 325 700802094H1 SATMON036 g1184773 BLASTN 382 1e−23 79 2048 325 700206976H1 SATMON003 g1184773 BLASTN 388 1e−23 87 2049 325 700799153H1 SATMON036 g293886 BLASTN 232 1e−22 92 2050 325 700456230H1 SATMON029 g1184771 BLASTN 333 1e−22 71 2051 325 700354919H1 SATMON024 g1184771 BLASTN 230 1e−20 100 2052 325 700614147H1 SATMON033 g22237 BLASTN 256 1e−18 91 2053 325 701181137H1 SATMONN06 g22237 BLASTN 322 1e−18 97 2054 325 700458047H1 SATMON029 g1184771 BLASTN 275 1e−14 100 2055 325 700807468H1 SATMON036 g1184773 BLASTN 179 1e−13 92 2056 3520 700212510H1 SATMON016 g168478 BLASTN 1590 1e−123 99 2057 3520 700097780H1 SATMON009 g168520 BLASTN 637 1e−122 97 2058 3520 700101968H1 SATMON009 g168520 BLASTN 1002 1e−117 98 2059 3520 700099736H1 SATMON009 g168520 BLASTN 1030 1e−116 97 2060 3520 700096850H1 SATMON008 g168520 BLASTN 938 1e−115 97 2061 3520 700101454H1 SATMON009 g168520 BLASTN 977 1e−115 97 2062 3520 700092378H1 SATMON008 g168520 BLASTN 651 1e−114 98 2063 3520 700099257H1 SATMON009 g22239 BLASTN 1478 1e−114 99 2064 3520 700209837H1 SATMON016 g168520 BLASTN 1012 1e−112 99 2065 3520 700097148H1 SATMON009 g168520 BLASTN 1030 1e−112 97 2066 3520 700100043H1 SATMON009 g168520 BLASTN 888 1e−111 96 2067 3520 700099516H1 SATMON009 g168520 BLASTN 991 1e−111 95 2068 3520 700097454H1 SATMON009 g168520 BLASTN 1028 1e−111 98 2069 3520 700099582H1 SATMON009 g168520 BLASTN 873 1e−109 98 2070 3520 700101028H1 SATMON009 g168520 BLASTN 963 1e−109 97 2071 3520 700101288H1 SATMON009 g168520 BLASTN 967 1e−109 98 2072 3520 700098981H1 SATMON009 g168520 BLASTN 1023 1e−109 98 2073 3520 700053377H1 SATMON009 g168478 BLASTN 1420 1e−109 100 2074 3520 700101538H1 SATMON009 g168520 BLASTN 958 1e−108 98 2075 3520 700093413H1 SATMON008 g168520 BLASTN 1037 1e−108 99 2076 3520 700098960H1 SATMON009 g168478 BLASTN 1004 1e−106 96 2077 3520 700212674H1 SATMON016 g168520 BLASTN 977 1e−105 98 2078 3520 700098986H1 SATMON009 g168478 BLASTN 1033 1e−105 98 2079 3520 700099244H1 SATMON009 g168520 BLASTN 976 1e−104 98 2080 3520 700100392H1 SATMON009 g168520 BLASTN 1002 1e−104 96 2081 3520 700044021H1 SATMON004 g168478 BLASTN 1350 1e−103 98 2082 3520 700043432H1 SATMON004 g168520 BLASTN 950 1e−102 97 2083 3520 700045175H1 SATMON004 g168520 BLASTN 963 1e−102 99 2084 3520 700099592H1 SATMON009 g168520 BLASTN 972 1e−102 94 2085 3520 700101559H1 SATMON009 g168478 BLASTN 1236 1e−102 94 2086 3520 700045717H1 SATMON004 g168478 BLASTN 1337 1e−102 96 2087 3520 700100711H1 SATMON009 g168520 BLASTN 996 1e−101 96 2088 3520 700098021H1 SATMON009 g168478 BLASTN 1189 1e−101 99 2089 3520 700044254H1 SATMON004 g22239 BLASTN 1327 1e−101 98 2090 3520 700041717H1 SATMON004 g168520 BLASTN 1010 1e−100 97 2091 3520 700044347H1 SATMON004 g168520 BLASTN 1028 1e−99 98 2092 3520 700097318H1 SATMON009 g168478 BLASTN 1121 1e−99 97 2093 3520 700045244H1 SATMON004 g22239 BLASTN 1295 1e−99 98 2094 3520 700041539H1 SATMON004 g168478 BLASTN 1300 1e−99 100 2095 3520 700100339H1 SATMON009 g168520 BLASTN 1014 1e−98 97 2096 3520 700099768H1 SATMON009 g168520 BLASTN 519 1e−97 96 2097 3520 700043795H1 SATMON004 g168520 BLASTN 973 1e−97 97 2098 3520 700043117H1 SATMON004 g168520 BLASTN 1007 1e−97 97 2099 3520 700211227H1 SATMON016 g168520 BLASTN 694 1e−96 92 2100 3520 700044187H1 SATMON004 g168520 BLASTN 958 1e−96 98 2101 3520 700025676H1 SATMON004 g168478 BLASTN 1259 1e−95 98 2102 3520 700094879H1 SATMON008 g168478 BLASTN 843 1e−94 95 2103 3520 700217617H1 SATMON016 g168520 BLASTN 898 1e−94 93 2104 3520 700404848H1 SATMON026 g168520 BLASTN 1039 1e−94 88 2105 3520 700044959H1 SATMON004 g168520 BLASTN 1000 1e−93 95 2106 3520 700213689H1 SATMON016 g168520 BLASTN 1007 1e−93 97 2107 3520 700210347H1 SATMON016 g168520 BLASTN 1191 1e−92 90 2108 3520 700045145H1 SATMON004 g168520 BLASTN 988 1e−91 98 2109 3520 700217745H1 SATMON016 g168520 BLASTN 1037 1e−91 98 2110 3520 700099288H1 SATMON009 g168478 BLASTN 1120 1e−91 93 2111 3520 700099630H1 SATMON009 g168520 BLASTN 445 1e−88 92 2112 3520 700214977H1 SATMON016 g22239 BLASTN 1084 1e−88 96 2113 3520 700045545H1 SATMON004 g22239 BLASTN 1161 1e−88 95 2114 3520 700198007H1 SATMON016 g22239 BLASTN 1167 1e−88 99 2115 3520 700216050H1 SATMON016 g168520 BLASTN 681 1e−85 88 2116 3520 700214595H1 SATMON016 g168478 BLASTN 975 1e−84 98 2117 3520 700215383H1 SATMON016 g168478 BLASTN 1021 1e−84 98 2118 3520 700098015H1 SATMON009 g168478 BLASTN 1080 1e−81 79 2119 3520 700210596H1 SATMON016 g168520 BLASTN 575 1e−79 92 2120 3520 700440284H1 SATMON026 g168478 BLASTN 914 1e−76 93 2121 3520 700215096H1 SATMON016 g168478 BLASTN 866 1e−75 95 2122 3520 700207885H1 SATMON016 g168520 BLASTN 408 1e−70 97 2123 3520 700044936H1 SATMON004 g168520 BLASTN 414 1e−68 89 2124 3520 700042261H1 SATMON004 g22239 BLASTN 579 1e−67 97 2125 3520 700213316H1 SATMON016 g22239 BLASTN 742 1e−53 98 2126 3520 700101372H1 SATMON009 g22239 BLASTN 625 1e−43 100 2127 3520 700053328H1 SATMON009 g168478 BLASTN 628 1e−43 99 2128 3520 700100601H1 SATMON009 g168478 BLASTN 610 1e−41 97 2129 3520 700101784H1 SATMON009 g168520 BLASTN 495 1e−40 99 2130 3520 700100849H1 SATMON009 g168520 BLASTN 505 1e−33 100 2131 3520 700098705H1 SATMON009 g168520 BLASTN 445 1e−32 99 2132 3520 700098336H1 SATMON009 g168478 BLASTN 450 1e−28 90 2133 3520 700404788H1 SATMON026 g22239 BLASTN 413 1e−25 96 2134 3520 700097106H1 SATMON009 g168520 BLASTN 300 1e−16 100 2135 4750 700267791H1 SATMON017 g1100222 BLASTN 685 1e−48 69 2136 4750 700346835H1 SATMON021 g1100222 BLASTN 689 1e−48 71 2137 4750 700205354H1 SATMON003 g1100222 BLASTN 576 1e−39 66 2138 4750 700213067H1 SATMON016 g1100222 BLASTN 558 1e−37 69 2139 4750 700073493H1 SATMON007 g1100222 BLASTN 513 1e−32 68 2140 482 700281924H2 SATMON021 g1100224 BLASTN 835 1e−60 79 2141 482 700076167H1 SATMON007 g1100224 BLASTN 765 1e−54 78 2142 482 700106880H1 SATMON010 g1100222 BLASTN 713 1e−50 79 2143 482 700343834H1 SATMON021 g1100224 BLASTN 650 1e−45 79 2144 482 700612539H1 SATMON033 g1100224 BLASTN 584 1e−39 80 2145 482 700017623H1 SATMON001 g1100224 BLASTN 535 1e−35 81 2146 5054 700043423H1 SATMON004 g1185553 BLASTN 241 1e−9 90 2147 5609 700098586H1 SATMON009 g2331136 BLASTN 1069 1e−80 80 2148 5609 700101965H1 SATMON009 g2331136 BLASTN 973 1e−72 78 2149 5609 700097652H1 SATMON009 g22239 BLASTN 530 1e−70 77 2150 5609 700045073H1 SATMON004 g2331136 BLASTN 908 1e−67 83 2151 5609 700100461H1 SATMON009 g2331136 BLASTN 896 1e−66 84 2152 5609 700100784H1 SATMON009 g22239 BLASTN 306 1e−65 79 2153 5609 700041674H1 SATMON004 g22239 BLASTN 893 1e−65 81 2154 5609 700101071H1 SATMON009 g22239 BLASTN 867 1e−63 79 2155 5609 700099485H1 SATMON009 g168478 BLASTN 462 1e−61 83 2156 5609 700101345H1 SATMON009 g2331136 BLASTN 744 1e−61 78 2157 5609 700043784H1 SATMON004 g22239 BLASTN 842 1e−61 80 2158 5609 700099589H1 SATMON009 g2331136 BLASTN 707 1e−60 76 2159 5609 700099264H1 SATMON009 g168478 BLASTN 568 1e−58 78 2160 5609 700041766H1 SATMON004 g168478 BLASTN 615 1e−58 86 2161 5609 700098403H1 SATMON009 g168521 BLASTN 798 1e−58 80 2162 5609 700042111H1 SATMON004 g21251 BLASTN 791 1e−57 75 2163 5609 700042979H1 SATMON004 g21251 BLASTN 783 1e−56 75 2164 5609 700579708H1 SATMON031 g21251 BLASTN 770 1e−55 76 2165 5609 700097230H1 SATMON009 g1181547 BLASTN 677 1e−47 75 2166 5609 700097983H1 SATMON009 g1181547 BLASTN 644 1e−44 76 2167 5609 700099990H1 SATMON009 g22239 BLASTN 633 1e−43 78 2168 5609 700404886H1 SATMON026 g22239 BLASTN 621 1e−42 79 2169 5609 700101261H1 SATMON009 g22239 BLASTN 306 1e−41 78 2170 5609 700025513H1 SATMON004 g21251 BLASTN 592 1e−40 72 2171 5609 700042534H1 SATMON004 g1181547 BLASTN 575 1e−39 73 2172 5609 700404890H1 SATMON026 g168520 BLASTN 324 1e−27 81 2173 5609 700100028H1 SATMON009 g1181547 BLASTN 435 1e−25 77 2174 5609 700097683H1 SATMON009 g170239 BLASTX 211 1e−22 92 2175 5609 700045480H1 SATMON004 g170239 BLASTX 202 1e−20 92 2176 5609 700101596H1 SATMON009 g21252 BLASTX 129 1e−17 80 2177 5609 700434377H1 SATMONN01 g168524 BLASTX 70 1e−16 94 2178 5609 700043206H1 SATMON004 g170239 BLASTX 150 1e−16 87 2179 5609 700025514H1 SATMON004 g21251 BLASTN 276 1e−14 69 2180 5609 700198075H1 SATMON016 g170239 BLASTX 138 1e−13 79 2181 5609 700100768H1 SATMON009 g21252 BLASTX 50 1e−10 78 2182 5609 700043373H1 SATMON004 g21252 BLASTX 67 1e−10 86 2183 5609 700097375H1 SATMON009 g21252 BLASTX 70 1e−9 77 2184 5609 700208045H1 SATMON016 g256965 BLASTX 72 1e−9 61 2185 7791 700426721H1 SATMONN01 g1185553 BLASTN 273 1e−12 83 2186 9845 700573046H1 SATMON030 g1185555 BLASTN 283 1e−23 70 2187 -L1431834 LIB143-029- LIB143 g22237 BLASTN 369 1e−65 94 Q1-E1-H1 2188 -L1433328 LIB143-020- LIB143 g22237 BLASTN 269 1e−11 82 Q1-E1-F2 2189 -L1435669 LIB143-049- LIB143 g1184773 BLASTN 409 1e−48 82 Q1-E1-H3 2190 -L1435747 LIB143-049- LIB143 g1184775 BLASTN 161 1e−13 85 Q1-E1-H4 2191 -L1482841 LIB148-009- LIB148 g717080 BLASTN 683 1e−46 75 Q1-E1-G2 2192 -L1891511 LIB189-007- LIB189 g168478 BLASTN 186 1e−12 85 Q1-E1-B4 2193 -L1893431 LIB189-023- LIB189 g168520 BLASTN 780 1e−58 80 Q1-E1-B8 2194 -L30591771 LIB3059-004- LIB3059 g1184773 BLASTN 253 1e−10 79 Q1-K1-C3 2195 -L30592823 LIB3059-013- LIB3059 g1184775 BLASTN 876 1e−64 94 Q1-K1-B4 2196 -L30595676 LIB3059-059- LIB3059 g1912310 BLASTX 138 1e−27 82 Q1-K1-D6 2197 -L30596448 LIB3059-052- LIB3059 g22302 BLASTN 207 1e−13 70 Q1-K1-E5 2198 -L30596730 LIB3059-055- LIB3059 g717080 BLASTN 234 1e−10 78 Q1-K1-C8 2199 -L30601281 LIB3060-001- LIB3060 g168520 BLASTN 762 1e−77 84 Q1-K1-A9 2200 -L30601466 LIB3060-002- LIB3060 g22239 BLASTN 153 1e−9 76 Q1-K2-G3 2201 -L30602361 LIB3060-004- LIB3060 g168521 BLASTN 935 1e−71 93 Q1-K1-E12 2202 -L30603772 LIB3060-040- LIB3060 g168520 BLASTN 766 1e−78 87 Q1-K1-H9 2203 -L30604121 LIB3060-037- LIB3060 g168478 BLASTN 238 1e−9 70 Q1-K1-B8 2204 -L30604680 LIB3060-024- LIB3060 g168520 BLASTN 490 1e−57 81 Q1-K1-C10 2205 -L30604772 LIB3060-020- LIB3060 g22237 BLASTN 344 1e−19 75 Q1-K1-B1 2206 -L30605068 LIB3060-023- LIB3060 g21252 BLASTX 77 1e−25 55 Q1-K1-D10 2207 -L30614406 LIB3061-034- LIB3061 g1184773 BLASTN 138 1e−20 95 Q1-K1-H4 2208 -L30621659 LIB3062-004- LIB3062 g1185553 BLASTN 263 1e−10 73 Q1-K1-D3 2209 -L30624091 LIB3062-022- LIB3062 g1184771 BLASTN 457 1e−29 61 Q1-K1-G4 2210 -L30625111 LIB3062-047- LIB3062 g168478 BLASTN 268 1e−13 77 Q1-K1-F4 2211 -L30625390 LIB3062-045- LIB3062 g3059121 BLASTN 246 1e−9 71 Q1-K1-B5 2212 -L30625502 LIB3062-045- LIB3062 g1184771 BLASTN 749 1e−93 78 Q1-K1-H6 2213 -L30626082 LIB3062-057- LIB3062 g22237 BLASTN 344 1e−19 80 Q1-K1-A6 2214 -L30661786 LIB3066-011- LIB3066 g1185553 BLASTN 410 1e−25 84 Q1-K1-G4 2215 -L30662411 LIB3066-035- LIB3066 g1184773 BLASTN 270 1e−13 93 Q1-K1-C8 2216 -L30664919 LIB3066-021- LIB3066 g1185553 BLASTN 346 1e−30 87 Q1-K1-B3 2217 -L30672802 LIB3067-016- LIB3067 g1184771 BLASTN 681 1e−53 70 Q1-K1-F10 2218 -L30673570 LIB3067-005- LIB3067 g1185553 BLASTN 466 1e−29 92 Q1-K1-A12 2219 -L30675145 LIB3067-055- LIB3067 g22237 BLASTN 438 1e−27 79 Q1-K1-H11 2220 -L30681335 LIB3068-001- LIB3068 g169851 BLASTN 540 1e−34 68 Q1-K1-F4 2221 -L30683415 LIB3068-036- LIB3068 g1628381 BLASTX 78 1e−30 55 Q1-K1-F4 2222 -L30692589 LIB3069-019- LIB3069 g22238 BLASTX 132 1e−26 40 Q1-K1-H1 2223 -L30693586 LIB3069-025- LIB3069 g1185553 BLASTN 327 1e−15 86 Q1-K1-F9 2224 -L30784053 LIB3078-029- LIB3078 g168479 BLASTX 130 1e−32 47 Q1-K1-F12 2225 -L30784418 LIB3078-039- LIB3078 g2331136 BLASTN 566 1e−38 74 Q1-K1-A2 2226 -L30791369 LIB3079-001- LIB3079 g1184771 BLASTN 1199 1e−96 84 Q1-K1-G1 2227 -L361450 LIB36-002- LIB36 g168478 BLASTN 698 1e−48 77 Q1-E1-C8 2228 -L362980 LIB36-019- LIB36 g22239 BLASTN 409 1e−25 83 Q1-E1-H2 2229 -L363043 LIB36-015- LIB36 g1184771 BLASTN 312 1e−58 83 Q1-E1-G8 2230 -L831348 LIB83-003- LIB83 g168478 BLASTN 286 1e−12 98 Q1-E1-A11 2231 -L832266 LIB83-007- LIB83 g1185555 BLASTN 381 1e−22 68 Q1-E1-C2 2232 -L841577 LIB84-027- LIB84 g168478 BLASTN 457 1e−29 95 Q1-E1-H4 2233 -L841855 LIB84-030- LIB84 g1185555 BLASTN 231 1e−10 75 Q1-E1-C10 2234 -L84758 LIB84-016- LIB84 g474407 BLASTN 1346 1e−133 97 Q1-E1-E5 2235 12126 LIB3062-056- LIB3062 g169851 BLASTN 890 1e−65 71 Q1-K1-C9 2236 1334 LIB143-061- LIB143 g717080 BLASTN 310 1e−14 83 Q1-E1-G2 2237 1334 LIB84-012- LIB84 g717080 BLASTN 289 1e−12 79 Q1-E12-B5 2238 13427 LIB3067-056- LIB3067 g1185553 BLASTN 489 1e−30 88 Q1-K1-B4 2239 13947 LIB3061-037- LIB3061 g1185553 BLASTN 334 1e−16 83 Q1-K1-C8 2240 17968 LIB3059-042- LIB3059 g1184775 BLASTN 1641 1e−128 98 Q1-K1-G12 2241 2468 LIB84-002- LIB84 g168478 BLASTN 1251 1e−95 99 Q1-E1-A7 2242 2468 LIB83-001- LIB83 g22239 BLASTN 860 1e−62 100 Q1-E1-E4 2243 26686 LIB3069-013- LIB3069 g1184772 BLASTX 155 1e−29 42 Q1-K1-H10 2244 27323 LIB3078-024- LIB3078 g474407 BLASTN 1386 1e−106 99 Q1-K1-G1 2245 27323 LIB3069-038- LIB3069 g474407 BLASTN 1025 1e−93 99 Q1-K1-F4 2246 27785 LIB148-039- LIB148 g1185553 BLASTN 495 1e−30 83 Q1-E1-A11 2247 27785 LIB148-006- LIB148 g1185553 BLASTN 267 1e−10 79 Q1-E1-B8 2248 29041 LIB148-017- LIB148 g1185553 BLASTN 410 1e−27 86 Q1-E1-D6 2249 29041 LIB148-024- LIB148 g1185553 BLASTN 441 1e−27 86 Q1-E1-C10 2250 29041 LIB148-058- LIB148 g1185553 BLASTN 441 1e−27 86 Q1-E1-D8 2251 29041 LIB143-040- LIB143 g1185553 BLASTN 441 1e−26 86 Q1-E1-H8 2252 30017 LIB148-057- LIB148 g717080 BLASTN 264 1e−10 65 Q1-E1-H7 2253 30327 LIB36-012- LIB36 g22302 BLASTN 266 1e−30 83 Q1-E1-B4 2254 31280 LIB36-002- LIB36 g1185553 BLASTN 337 1e−16 79 Q1-E1-A4 2255 32165 LIB36-013- LIB36 g474407 BLASTN 1417 1e−109 91 Q1-E1-F8 2256 325 LIB3062-009- LIB3062 g22237 BLASTN 2130 1e−169 100 Q1-K1-B6 2257 325 LIB3059-029- LIB3059 g1184771 BLASTN 2098 1e−166 98 Q1-K1-E5 2258 325 LIB3066-001- LIB3066 g1184773 BLASTN 2063 1e−163 95 Q1-K1-C3 2259 325 LIB3067-029- LIB3067 g1184775 BLASTN 1334 1e−162 96 Q1-K1-F10 2260 325 LIB3062-012- LIB3062 g22237 BLASTN 1952 1e−162 99 Q1-K1-C5 2261 325 LIB3061-011- LIB3061 g1184773 BLASTN 1973 1e−160 99 Q1-K1-H1 2262 325 LIB3061-034- LIB3061 g1184773 BLASTN 2027 1e−160 98 Q1-K1-H6 2263 325 LIB3061-011- LIB3061 g22237 BLASTN 1691 1e−159 98 Q1-K1-D5 2264 325 LIB3068-026- LIB3068 g22237 BLASTN 1899 1e−159 98 Q1-K1-E3 2265 325 LIB3061-034- LIB3061 g1184773 BLASTN 1890 1e−158 98 Q1-K1-A7 2266 325 LIB143-006- LIB143 g1184773 BLASTN 1454 1e−157 95 Q1-E1-F5 2267 325 LIB3068-008- LIB3068 g1184771 BLASTN 1673 1e−157 94 Q1-K1-H2 2268 325 LIB3060-001- LIB3060 g1184771 BLASTN 1673 1e−155 96 Q1-K2-C11 2269 325 LIB3059-042- LIB3059 g1184773 BLASTN 1751 1e−154 97 Q1-K1-G11 2270 325 LIB3060-053- LIB3060 g1184771 BLASTN 1954 1e−154 99 Q1-K1-H6 2271 325 LIB3062-001- LIB3062 g22237 BLASTN 1836 1e−152 93 Q1-K2-B9 2272 325 LIB143-050- LIB143 g1184773 BLASTN 1837 1e−152 94 Q1-E1-C2 2273 325 LIB3059-002- LIB3059 g1184773 BLASTN 1933 1e−152 94 Q1-K2-D10 2274 325 LIB3066-021- LIB3066 g1184773 BLASTN 1482 1e−151 92 Q1-K1-G1 2275 325 LIB36-006- LIB36 g1184771 BLASTN 1915 1e−151 96 Q1-E1-G10 2276 325 LIB3061-013- LIB3061 g1184773 BLASTN 1918 1e−151 96 Q1-K1-D10 2277 325 LIB3062-035- LIB3062 g22237 BLASTN 849 1e−150 94 Q1-K1-B9 2278 325 LIB3068-002- LIB3068 g1184771 BLASTN 1056 1e−150 97 Q1-K1-D3 2279 325 LIB3059-030- LIB3059 g1184773 BLASTN 1912 1e−150 99 Q1-K1-E12 2280 325 LIB3059-048- LIB3059 g1184773 BLASTN 1649 1e−148 90 Q1-K1-D4 2281 325 LIB143-025- LIB143 g22237 BLASTN 1887 1e−148 94 Q1-E1-E8 2282 325 LIB143-057- LIB143 g1184773 BLASTN 1496 1e−146 95 Q1-E1-E6 2283 325 LIB143-015- LIB143 g1184771 BLASTN 1855 1e−146 100 Q1-E1-F12 2284 325 LIB3060-049- LIB3060 g1184771 BLASTN 1858 1e−146 99 Q1-K1-H7 2285 325 LIB143-025- LIB143 g1184771 BLASTN 1413 1e−142 95 Q1-E1-H7 2286 325 LIB84-027- LIB84 g22237 BLASTN 1654 1e−142 97 Q1-E1-F5 2287 325 LIB36-003- LIB36 g1184771 BLASTN 1536 1e−141 96 Q1-E1-C2 2288 325 LIB3067-032- LIB3067 g1184773 BLASTN 1121 1e−139 94 Q1-K1-B12 2289 325 LIB3069-038- LIB3069 g22237 BLASTN 1372 1e−137 90 Q1-K1-F9 2290 325 LIB3066-021- LIB3066 g1184773 BLASTN 1535 1e−136 94 Q1-K1-G2 2291 325 LIB3069-043- LIB3069 g22237 BLASTN 1483 1e−134 93 Q1-K1-A1 2292 325 LIB3060-020- LIB3060 g1184771 BLASTN 1110 1e−132 95 Q1-K1-A12 2293 325 LIB143-014- LIB143 g1184773 BLASTN 1625 1e−130 93 Q1-E1-F8 2294 325 LIB3066-021- LIB3066 g1184773 BLASTN 1221 1e−127 86 Q1-K1-G3 2295 325 LIB3066-004- LIB3066 g1184771 BLASTN 1482 1e−125 91 Q1-K1-G9 2296 325 LIB143-055- LIB143 g1184771 BLASTN 1503 1e−125 87 Q1-E1-B3 2297 325 LIB3060-046- LIB3060 g1184771 BLASTN 1315 1e−124 95 Q1-K1-C4 2298 325 LIB3060-012- LIB3060 g22237 BLASTN 1432 1e−123 94 Q1-K1-E9 2299 325 LIB3066-037- LIB3066 g1184771 BLASTN 837 1e−121 90 Q1-K1-A2 2300 325 LIB3067-031- LIB3067 g1184773 BLASTN 923 1e−121 90 Q1-K1-G12 2301 325 LIB143-049- LIB143 g1184771 BLASTN 1497 1e−119 99 Q1-E1-D6 2302 325 LIB3060-022- LIB3060 g22237 BLASTN 1168 1e−117 89 Q1-K1-E7 2303 325 LIB143-012- LIB143 g1184773 BLASTN 1501 1e−116 95 Q1-E1-C2 2304 325 LIB36-006- LIB36 g22237 BLASTN 1464 1e−113 95 Q1-E1-D9 2305 325 LIB3060-001- LIB3060 g1184771 BLASTN 981 1e−112 88 Q1-K2-C12 2306 325 LIB143-063- LIB143 g1184773 BLASTN 1354 1e−110 87 Q1-E1-G8 2307 325 LIB3060-028- LIB3060 g22237 BLASTN 613 1e−109 93 Q1-K1-E1 2308 325 LIB3061-001- LIB3061 g1184771 BLASTN 743 1e−107 86 Q1-K2-H1 2309 325 LIB143-017- LIB143 g1184773 BLASTN 1217 1e−107 92 Q1-E1-G4 2310 325 30-LIB84- LIB84 g1184771 BLASTN 988 1e−106 95 007-Q1-E1-H5 2311 325 LIB3061-056- LIB3061 g1184773 BLASTN 1382 1e−106 89 Q1-K1-F11 2312 325 LIB3062-023- LIB3062 g22237 BLASTN 1373 1e−105 79 Q1-K1-F7 2313 325 LIB3068-055- LIB3068 g1184771 BLASTN 566 1e−101 90 Q1-K1-G2 2314 325 LIB143-050- LIB143 g1184773 BLASTN 980 1e−100 87 Q1-E1-C3 2315 325 LIB3061-005- LIB3061 g1184773 BLASTN 816 1e−99 92 Q1-K1-B3 2316 325 LIB3068-051- LIB3068 g1184771 BLASTN 658 1e−95 96 Q1-K1-C5 2317 325 LIB3068-021- LIB3068 g22237 BLASTN 1074 1e−92 94 Q1-K1-C5 2318 325 LIB3059-002- LIB3059 g1184773 BLASTN 905 1e−91 86 Q1-K2-D11 2319 325 LIB143-029- LIB143 g22237 BLASTN 979 1e−91 96 Q1-E1-E1 2320 325 LIB3062-016- LIB3062 g1184775 BLASTN 1164 1e−91 98 Q1-K1-E1 2321 325 LIB3062-035- LIB3062 g1184771 BLASTN 1058 1e−89 90 Q1-K1-H4 2322 325 LIB189-023- LIB189 g22237 BLASTN 589 1e−88 87 Q1-E1-F1 2323 325 LIB143-067- LIB143 g1184771 BLASTN 777 1e−84 88 Q1-E1-H11 2324 325 LIB3061-024- LIB3061 g1184773 BLASTN 838 1e−78 94 Q1-K1-C11 2325 325 LIB3068-041- LIB3068 g1184771 BLASTN 680 1e−77 95 Q1-K1-B11 2326 325 LIB3068-026- LIB3068 g1184771 BLASTN 680 1e−69 94 Q1-K1-D5 2327 325 LIB3061-012- LIB3061 g1184773 BLASTN 744 1e−66 87 Q1-K1-C11 2328 325 LIB143-066- LIB143 g1184771 BLASTN 634 1e−64 93 Q1-E1-H11 2329 325 LIB3059-004- LIB3059 g1184771 BLASTN 818 1e−59 93 Q1-K1-G1 2330 325 LIB3069-053- LIB3069 g1184771 BLASTN 347 1e−46 89 Q1-K1-D10 2331 325 LIB143-021- LIB143 g1184773 BLASTN 367 1e−35 90 Q1-E1-E2 2332 325 LIB3062-057- LIB3062 g22237 BLASTN 536 1e−35 99 Q1-K1-A8 2333 325 LIB189-019- LIB189 g1184773 BLASTN 485 1e−31 91 Q1-E1-C5 2334 325 LIB143-037- LIB143 g22237 BLASTN 486 1e−31 98 Q1-E1-C8 2335 325 LIB3059-012- LIB3059 g1184773 BLASTN 253 1e−12 98 Q1-K1-F6 2336 3520 LIB3078-050- LIB3078 g168478 BLASTN 2101 1e−166 94 Q1-K1-G8 2337 3520 LIB3060-041- LIB3060 g22239 BLASTN 2038 1e−161 95 Q1-K1-E8 2338 3520 LIB3078-055- LIB3078 g168478 BLASTN 1903 1e−149 92 Q1-K1-H5 2339 3520 LIB3060-001- LIB3060 g168520 BLASTN 1862 1e−148 98 Q1-K2-A9 2340 3520 LIB3060-043- LIB3060 g168520 BLASTN 1848 1e−147 97 Q1-K1-C11 2341 3520 LIB3060-003- LIB3060 g168520 BLASTN 1853 1e−147 97 Q1-K1-D9 2342 3520 LIB3060-041- LIB3060 g168520 BLASTN 1830 1e−145 97 Q1-K1-F6 2343 3520 LIB3060-043- LIB3060 g168520 BLASTN 1327 1e−144 96 Q1-K1-F2 2344 3520 LIB3060-047- LIB3060 g168520 BLASTN 1797 1e−143 97 Q1-K1-C9 2345 3520 LIB84-017- LIB84 g168520 BLASTN 1536 1e−142 97 Q1-E1-D3 2346 3520 LIB36-002- LIB36 g168520 BLASTN 1573 1e−142 97 Q1-E1-B8 2347 3520 LIB3060-029- LIB3060 g168520 BLASTN 1675 1e−140 97 Q1-K1-B7 2348 3520 LIB36-010- LIB36 g168520 BLASTN 1550 1e−139 96 Q1-E1-C7 2349 3520 LIB3060-042- LIB3060 g168520 BLASTN 1601 1e−139 97 Q1-K1-A10 2350 3520 LIB3060-018- LIB3060 g22239 BLASTN 1773 1e−139 95 Q1-K1-F11 2351 3520 LIB36-003- LIB36 g22239 BLASTN 1523 1e−137 98 Q1-E1-H7 2352 3520 LIB189-029- LIB189 g168520 BLASTN 1531 1e−136 96 Q1-E1-F9 2353 3520 LIB36-006- LIB36 g168478 BLASTN 1118 1e−130 96 Q1-E1-B1 2354 3520 LIB3060-021- LIB3060 g168520 BLASTN 1627 1e−129 96 Q1-K1-F4 2355 3520 LIB3060-037- LIB3060 g168520 BLASTN 1625 1e−128 95 Q1-K1-B6 2356 3520 LIB84-003- LIB84 g168520 BLASTN 726 1e−121 92 Q1-E1-C1 2357 3520 LIB36-021- LIB36 g168520 BLASTN 1537 1e−121 97 Q1-E1-H3 2358 3520 LIB3078-056- LIB3078 g22239 BLASTN 1539 1e−119 96 Q1-K1-G1 2359 3520 LIB3060-025- LIB3060 g168520 BLASTN 1416 1e−118 96 Q1-K1-B12 2360 3520 LIB189-004- LIB189 g168520 BLASTN 1499 1e−118 88 Q1-E1-F9 2361 3520 LIB3060-035- LIB3060 g168520 BLASTN 1339 1e−117 96 Q1-K1-A11 2362 3520 LIB3078-004- LIB3078 g22239 BLASTN 1256 1e−116 91 Q1-K1-D8 2363 3520 LIB36-009- LIB36 g168478 BLASTN 1318 1e−115 98 Q1-E1-H1 2364 3520 LIB3060-013- LIB3060 g168478 BLASTN 1205 1e−112 92 Q1-K1-F8 2365 3520 LIB3060-041- LIB3060 g168520 BLASTN 1332 1e−104 84 Q1-K1-G11 2366 3520 LIB3060-018- LIB3060 g22239 BLASTN 718 1e−100 90 Q1-K1-F10 2367 3520 LIB3060-008- LIB3060 g168520 BLASTN 532 1e−36 83 Q1-K1-F1 2368 3520 LIB3060-039- LIB3060 g168520 BLASTN 441 1e−35 88 Q1-K1-E4 2369 5609 LIB3060-016- LIB3060 g22239 BLASTN 787 1e−99 78 Q1-K1-F3 2370 5609 LIB36-020- LIB36 g168478 BLASTN 756 1e−91 81 Q1-E1-A6 2371 5609 LIB189-011- LIB189 g2331136 BLASTN 945 1e−90 77 Q1-E1-H7 2372 5609 LIB36-019- LIB36 g168478 BLASTN 950 1e−90 77 Q1-E1-B10 2373 5609 LIB3060-049- LIB3060 g336389 BLASTN 1076 1e−80 73 Q1-K1-A12 2374 5609 LIB36-021- LIB36 g168478 BLASTN 926 1e−76 79 Q1-E1-H8 2375 5609 LIB84-028- LIB84 g21251 BLASTN 866 1e−66 77 Q1-E1-H5 2376 5609 LIB3060-036- LIB3060 g21251 BLASTN 827 1e−60 70 Q1-K1-B9 2377 5609 LIB36-001- LIB36 g168478 BLASTN 680 1e−58 86 Q1-E1-A3 2378 5609 LIB189-017- LIB189 g21252 BLASTX 228 1e−52 68 Q1-E1-C6 2379 5609 LIB189-015- LIB189 g168478 BLASTN 430 1e−51 75 Q1-E1-C5 2380 5609 LIB3060-035- LIB3060 g21252 BLASTX 215 1e−49 72 Q1-K1-F2 2381 5609 LIB36-003- LIB36 g21252 BLASTX 222 1e−43 76 Q1-E1-D2 2382 5609 LIB3060-023- LIB3060 g21252 BLASTX 105 1e−41 68 Q1-K1-D9 2383 5609 LIB3060-018- LIB3060 g168520 BLASTN 254 1e−26 75 Q1-K1-E11 MAIZE PUTATIVE GLYCERALDEHYDE 3-PHOSPHATE DEHYDROGENASE 2384 5609 700043392H1 SATMON004 g168567 BLASTN 926 1e−70 98 2385 5609 700041871H1 SATMON004 g168567 BLASTN 738 1e−54 99 2386 5609 700426511H1 SATMONN01 g168567 BLASTN 625 1e−45 100 2387 5609 700044710H1 SATMON004 g168567 BLASTN 570 1e−40 100 2388 5609 700216320H1 SATMON016 g168567 BLASTN 571 1e−40 99 2389 5609 700216328H1 SATMON016 g168567 BLASTN 413 1e−26 98 2390 5609 LIB36-006- LIB36 g168567 BLASTN 931 1e−70 99 Q1-E1-A7 2391 5609 LIB189-010- LIB189 g168567 BLASTN 915 1e−69 98 Q1-E1-F11 2392 5609 LIB83-006- LIB83 g168567 BLASTN 917 1e−69 98 Q1-E1-H8 2393 5609 LIB36-017- LIB36 g168567 BLASTN 486 1e−68 96 Q1-E1-A1 2394 5609 LIB3078-014- LIB3078 g168567 BLASTN 906 1e−68 97 Q1-K1-H3 2395 5609 LIB189-022- LIB189 g168567 BLASTN 931 1e−70 99 Q1-E1-H11 2396 5609 LIB3078-002- LIB3078 g168567 BLASTN 880 1e−66 97 Q1-K1-B8 SOYBEAN GLYCERALDEHYDE 3-PHOSPHATE DEHYDROGENASE 2397 -700556687 700556687H1 SOYMON001 g2905771 BLASTN 315 1e−27 91 2398 -700652993 700652993H1 SOYMON003 g20732 BLASTN 538 1e−34 84 2399 -700669859 700669859H1 SOYMON006 g19565 BLASTN 404 1e−24 78 2400 -700682023 700682023H1 SOYMON008 g1184775 BLASTN 659 1e−89 95 2401 -700739645 700739645H1 SOYMON012 g20732 BLASTN 906 1e−70 91 2402 -700744137 700744137H1 SOYMON013 g12158 BLASTN 344 1e−32 77 2403 -700749096 700749096H1 SOYMON013 g425795 BLASTN 337 1e−17 75 2404 -700763386 700763386H1 SOYMON015 g20550 BLASTN 560 1e−37 80 2405 -700854894 700854894H1 SOYMON023 g1184771 BLASTN 300 1e−19 79 2406 -700870634 700870634H1 SOYMON018 g20728 BLASTN 374 1e−21 68 2407 -700871731 700871731H1 SOYMON018 g309671 BLASTX 76 1e−8 49 2408 -700891638 700891638H1 SOYMON024 g496493 BLASTN 771 1e−55 82 2409 -700954983 700954983H1 SOYMON022 g1185556 BLASTX 131 1e−17 86 2410 -700961364 700961364H1 SOYMON022 g20732 BLASTN 267 1e−11 88 2411 -700961396 700961396H1 SOYMON022 g20732 BLASTN 330 1e−17 87 2412 -700963442 700963442H1 SOYMON022 g169090 BLASTN 485 1e−31 77 2413 -700984474 700984474H1 SOYMON009 g167293 BLASTN 432 1e−51 81 2414 -700989533 700989533H1 SOYMON011 g496493 BLASTN 1057 1e−79 90 2415 -700990284 700990284H1 SOYMON011 g2331137 BLASTX 177 1e−17 88 2416 -700991120 700991120H1 SOYMON011 g2905771 BLASTN 262 1e−11 96 2417 -700991826 700991826H1 SOYMON011 g20732 BLASTN 344 1e−29 71 2418 -700993359 700993359H1 SOYMON011 g19565 BLASTN 620 1e−42 76 2419 -701000288 701000288H1 SOYMON018 g20728 BLASTN 550 1e−43 77 2420 -701049142 701049142H1 SOYMON032 g3059121 BLASTN 612 1e−42 67 2421 -701049262 701049262H1 SOYMON032 g1100222 BLASTN 781 1e−56 77 2422 -701064532 701064532H1 SOYMON034 g19565 BLASTN 345 1e−19 87 2423 -701107753 701107753H1 SOYMON036 g496493 BLASTN 773 1e−55 77 2424 -701128594 701128594H1 SOYMON037 g19565 BLASTN 489 1e−31 83 2425 -701140262 701140262H1 SOYMON038 g169090 BLASTN 449 1e−28 85 2426 -701146678 701146678H1 SOYMON031 g2078298 BLASTX 52 1e−10 66 2427 -701151833 701151833H1 SOYMON031 g1931618 BLASTN 567 1e−38 81 2428 -701203691 701203691H2 SOYMON035 g169090 BLASTN 264 1e−11 87 2429 -701208478 701208478H1 SOYMON035 g169090 BLASTN 262 1e−22 69 2430 1061 700763870H1 SOYMON018 g20728 BLASTN 1054 1e−91 88 2431 1061 700556966H1 SOYMON001 g20728 BLASTN 1199 1e−91 91 2432 1061 700980735H1 SOYMON009 g20728 BLASTN 1140 1e−86 89 2433 1061 700983864H1 SOYMON009 g20728 BLASTN 1147 1e−86 88 2434 1061 700786535H1 SOYMON011 g12158 BLASTN 1086 1e−81 86 2435 1061 700728027H1 SOYMON009 g20728 BLASTN 767 1e−79 89 2436 1061 700684426H1 SOYMON008 g20728 BLASTN 1045 1e−78 90 2437 1061 700559635H1 SOYMON001 g20728 BLASTN 799 1e−77 85 2438 1061 700555476H1 SOYMON001 g20728 BLASTN 891 1e−77 87 2439 1061 700876005H1 SOYMON018 g20728 BLASTN 595 1e−76 88 2440 1061 700646201H1 SOYMON012 g12158 BLASTN 784 1e−75 88 2441 1061 700873429H1 SOYMON018 g20728 BLASTN 853 1e−75 88 2442 1061 700685875H1 SOYMON008 g20728 BLASTN 894 1e−75 89 2443 1061 700554131H1 SOYMON001 g20728 BLASTN 925 1e−75 88 2444 1061 700686559H1 SOYMON008 g20728 BLASTN 1012 1e−75 86 2445 1061 700873329H1 SOYMON018 g20728 BLASTN 1013 1e−75 89 2446 1061 701061532H1 SOYMON033 g20728 BLASTN 1017 1e−75 88 2447 1061 700876258H1 SOYMON018 g20728 BLASTN 562 1e−73 91 2448 1061 700991748H1 SOYMON011 g20728 BLASTN 646 1e−73 85 2449 1061 700752804H1 SOYMON014 g20728 BLASTN 984 1e−73 86 2450 1061 700873301H1 SOYMON018 g20728 BLASTN 988 1e−73 87 2451 1061 700977867H1 SOYMON009 g20728 BLASTN 974 1e−72 86 2452 1061 700558508H1 SOYMON001 g12158 BLASTN 562 1e−71 85 2453 1061 700558346H1 SOYMON001 g12158 BLASTN 800 1e−71 89 2454 1061 701104595H1 SOYMON036 g20728 BLASTN 958 1e−71 85 2455 1061 701107372H1 SOYMON036 g20728 BLASTN 959 1e−71 83 2456 1061 700877182H1 SOYMON018 g20728 BLASTN 963 1e−71 85 2457 1061 700682345H2 SOYMON008 g20728 BLASTN 965 1e−71 87 2458 1061 700999844H1 SOYMON018 g20728 BLASTN 965 1e−71 85 2459 1061 700962204H1 SOYMON022 g12158 BLASTN 968 1e−71 85 2460 1061 700962351H1 SOYMON022 g20728 BLASTN 525 1e−69 86 2461 1061 700743037H1 SOYMON012 g20728 BLASTN 563 1e−69 85 2462 1061 700975367H1 SOYMON009 g20728 BLASTN 938 1e−69 84 2463 1061 700844411H1 SOYMON021 g20728 BLASTN 944 1e−69 92 2464 1061 700891407H1 SOYMON024 g12158 BLASTN 946 1e−69 87 2465 1061 700556475H1 SOYMON001 g20728 BLASTN 743 1e−68 85 2466 1061 700739632H1 SOYMON012 g20728 BLASTN 849 1e−68 83 2467 1061 700752141H1 SOYMON014 g12158 BLASTN 928 1e−68 85 2468 1061 700654954H1 SOYMON004 g20728 BLASTN 932 1e−68 83 2469 1061 700874388H1 SOYMON018 g12158 BLASTN 932 1e−68 88 2470 1061 701156507H1 SOYMON031 g20728 BLASTN 485 1e−67 88 2471 1061 700646112H1 SOYMON012 g20728 BLASTN 715 1e−67 86 2472 1061 700873965H1 SOYMON018 g20728 BLASTN 911 1e−67 85 2473 1061 700741948H1 SOYMON012 g20728 BLASTN 898 1e−66 86 2474 1061 700875513H1 SOYMON018 g20728 BLASTN 900 1e−66 87 2475 1061 700874967H1 SOYMON018 g20728 BLASTN 546 1e−65 86 2476 1061 700559242H1 SOYMON001 g20728 BLASTN 743 1e−65 84 2477 1061 700559801H1 SOYMON001 g20728 BLASTN 743 1e−65 84 2478 1061 700659588H1 SOYMON004 g12158 BLASTN 888 1e−65 84 2479 1061 700725516H1 SOYMON009 g12158 BLASTN 495 1e−64 87 2480 1061 700901411H1 SOYMON027 g20728 BLASTN 793 1e−64 87 2481 1061 700790272H2 SOYMON011 g12158 BLASTN 883 1e−64 84 2482 1061 700942783H1 SOYMON024 g12158 BLASTN 507 1e−63 86 2483 1061 700876055H1 SOYMON018 g20728 BLASTN 535 1e−63 85 2484 1061 700554719H1 SOYMON001 g20728 BLASTN 726 1e−63 85 2485 1061 700993112H1 SOYMON011 g20728 BLASTN 402 1e−62 85 2486 1061 700684688H1 SOYMON008 g12158 BLASTN 519 1e−62 84 2487 1061 700890177H1 SOYMON024 g20728 BLASTN 579 1e−62 85 2488 1061 700554380H1 SOYMON001 g20728 BLASTN 712 1e−62 84 2489 1061 700876338H1 SOYMON018 g12158 BLASTN 856 1e−62 86 2490 1061 700993901H1 SOYMON011 g20728 BLASTN 583 1e−61 88 2491 1061 701103760H1 SOYMON036 g12158 BLASTN 843 1e−61 80 2492 1061 700684581H1 SOYMON008 g12158 BLASTN 850 1e−61 83 2493 1061 701049681H1 SOYMON032 g20728 BLASTN 545 1e−60 84 2494 1061 700681925H1 SOYMON008 g20728 BLASTN 355 1e−59 81 2495 1061 700680184H2 SOYMON008 g20728 BLASTN 478 1e−59 85 2496 1061 701108645H1 SOYMON036 g12158 BLASTN 775 1e−55 85 2497 1061 701106940H1 SOYMON036 g12158 BLASTN 775 1e−55 85 2498 1061 700984503H1 SOYMON009 g20728 BLASTN 516 1e−54 83 2499 1061 700738754H1 SOYMON012 g166701 BLASTN 759 1e−54 78 2500 1061 700685581H1 SOYMON008 g12158 BLASTN 375 1e−53 85 2501 1061 700977296H1 SOYMON009 g12158 BLASTN 470 1e−53 82 2502 1061 700999412H1 SOYMON018 g166701 BLASTN 617 1e−53 80 2503 1061 700898819H1 SOYMON027 g12158 BLASTN 722 1e−53 81 2504 1061 700994354H1 SOYMON011 g20728 BLASTN 743 1e−53 85 2505 1061 700685709H1 SOYMON008 g20728 BLASTN 743 1e−53 85 2506 1061 700738315H1 SOYMON012 g20728 BLASTN 743 1e−53 85 2507 1061 700873275H1 SOYMON018 g20728 BLASTN 743 1e−53 85 2508 1061 700555226H1 SOYMON001 g20728 BLASTN 743 1e−53 85 2509 1061 700892169H1 SOYMON024 g20728 BLASTN 743 1e−53 85 2510 1061 701107458H1 SOYMON036 g20728 BLASTN 743 1e−53 85 2511 1061 701047451H1 SOYMON032 g20728 BLASTN 743 1e−53 85 2512 1061 700994065H1 SOYMON011 g20728 BLASTN 744 1e−53 86 2513 1061 700968347H1 SOYMON036 g20728 BLASTN 746 1e−53 85 2514 1061 700740108H1 SOYMON012 g20728 BLASTN 732 1e−52 88 2515 1061 700556578H1 SOYMON001 g20728 BLASTN 735 1e−52 86 2516 1061 700646223H1 SOYMON012 g20728 BLASTN 735 1e−52 86 2517 1061 700686442H1 SOYMON008 g20728 BLASTN 735 1e−52 86 2518 1061 700995540H1 SOYMON011 g20728 BLASTN 735 1e−52 86 2519 1061 700997359H1 SOYMON018 g20728 BLASTN 735 1e−52 86 2520 1061 700863529H1 SOYMON027 g20728 BLASTN 735 1e−52 86 2521 1061 700874946H1 SOYMON018 g20728 BLASTN 735 1e−52 86 2522 1061 700789664H2 SOYMON011 g20728 BLASTN 735 1e−52 86 2523 1061 700559731H1 SOYMON001 g20728 BLASTN 735 1e−52 86 2524 1061 701141680H1 SOYMON038 g20728 BLASTN 735 1e−52 86 2525 1061 700555668H1 SOYMON001 g20728 BLASTN 735 1e−52 86 2526 1061 700553965H1 SOYMON001 g20728 BLASTN 735 1e−52 86 2527 1061 700989276H1 SOYMON011 g20728 BLASTN 735 1e−52 86 2528 1061 701213488H1 SOYMON035 g20728 BLASTN 735 1e−52 86 2529 1061 701120382H1 SOYMON037 g20728 BLASTN 735 1e−52 86 2530 1061 700740875H1 SOYMON012 g20728 BLASTN 735 1e−52 86 2531 1061 700741835H1 SOYMON012 g20728 BLASTN 736 1e−52 85 2532 1061 700995653H1 SOYMON011 g20728 BLASTN 736 1e−52 85 2533 1061 700906218H1 SOYMON022 g20728 BLASTN 736 1e−52 85 2534 1061 700684347H1 SOYMON008 g20728 BLASTN 736 1e−52 85 2535 1061 700728605H1 SOYMON009 g20728 BLASTN 737 1e−52 86 2536 1061 700789578H2 SOYMON011 g20728 BLASTN 740 1e−52 87 2537 1061 700787421H2 SOYMON011 g20728 BLASTN 718 1e−51 84 2538 1061 700560934H1 SOYMON001 g20728 BLASTN 719 1e−51 84 2539 1061 700876650H1 SOYMON018 g20728 BLASTN 722 1e−51 84 2540 1061 700740868H1 SOYMON012 g20728 BLASTN 722 1e−51 84 2541 1061 700741374H1 SOYMON012 g20728 BLASTN 722 1e−51 84 2542 1061 700994074H1 SOYMON011 g20728 BLASTN 723 1e−51 86 2543 1061 701109502H1 SOYMON036 g20728 BLASTN 728 1e−51 86 2544 1061 700875104H1 SOYMON018 g20728 BLASTN 728 1e−51 86 2545 1061 700786270H2 SOYMON011 g20728 BLASTN 728 1e−51 86 2546 1061 700556484H1 SOYMON001 g20728 BLASTN 729 1e−51 84 2547 1061 700998979H1 SOYMON018 g20728 BLASTN 729 1e−51 84 2548 1061 701109358H1 SOYMON036 g20728 BLASTN 729 1e−51 84 2549 1061 700763760H1 SOYMON018 g12158 BLASTN 730 1e−51 83 2550 1061 701001681H1 SOYMON018 g20728 BLASTN 422 1e−50 85 2551 1061 700991945H1 SOYMON011 g20728 BLASTN 706 1e−50 83 2552 1061 700789781H1 SOYMON011 g20728 BLASTN 709 1e−50 87 2553 1061 700554372H1 SOYMON001 g20728 BLASTN 709 1e−50 83 2554 1061 700993753H1 SOYMON011 g12158 BLASTN 709 1e−50 87 2555 1061 700876992H1 SOYMON018 g20728 BLASTN 714 1e−50 85 2556 1061 700960223H1 SOYMON022 g20728 BLASTN 714 1e−50 85 2557 1061 700686495H1 SOYMON008 g20728 BLASTN 717 1e−50 85 2558 1061 700557711H1 SOYMON001 g20728 BLASTN 469 1e−49 83 2559 1061 700984028H1 SOYMON009 g20728 BLASTN 560 1e−49 82 2560 1061 700556584H1 SOYMON001 g20728 BLASTN 563 1e−49 86 2561 1061 700870942H1 SOYMON018 g20728 BLASTN 576 1e−49 78 2562 1061 700871710H1 SOYMON018 g166701 BLASTN 695 1e−49 79 2563 1061 700738589H1 SOYMON012 g20728 BLASTN 697 1e−49 86 2564 1061 700738856H1 SOYMON012 g20728 BLASTN 704 1e−49 86 2565 1061 701002335H1 SOYMON018 g20728 BLASTN 704 1e−49 85 2566 1061 701001628H1 SOYMON018 g20728 BLASTN 704 1e−49 85 2567 1061 700787485H2 SOYMON011 g20728 BLASTN 415 1e−48 83 2568 1061 700683818H1 SOYMON008 g12158 BLASTN 442 1e−48 82 2569 1061 700554247H1 SOYMON001 g20728 BLASTN 480 1e−48 84 2570 1061 700744021H1 SOYMON012 g20728 BLASTN 554 1e−48 84 2571 1061 700787533H1 SOYMON011 g20728 BLASTN 573 1e−48 84 2572 1061 700985942H1 SOYMON009 g20728 BLASTN 598 1e−48 85 2573 1061 701104728H1 SOYMON036 g20728 BLASTN 609 1e−48 83 2574 1061 700988933H1 SOYMON011 g20728 BLASTN 637 1e−48 85 2575 1061 701109795H1 SOYMON036 g20728 BLASTN 644 1e−48 87 2576 1061 700984329H1 SOYMON009 g20728 BLASTN 655 1e−48 86 2577 1061 701000601H1 SOYMON018 g20728 BLASTN 682 1e−48 86 2578 1061 700686572H1 SOYMON008 g20728 BLASTN 684 1e−48 86 2579 1061 700791971H1 SOYMON011 g20728 BLASTN 692 1e−48 86 2580 1061 700740621H1 SOYMON012 g20728 BLASTN 343 1e−47 84 2581 1061 700994492H1 SOYMON011 g20728 BLASTN 413 1e−47 86 2582 1061 701108677H1 SOYMON036 g20728 BLASTN 553 1e−47 85 2583 1061 700740371H1 SOYMON012 g12158 BLASTN 640 1e−47 84 2584 1061 700737944H1 SOYMON012 g20728 BLASTN 670 1e−47 81 2585 1061 700788840H2 SOYMON011 g20728 BLASTN 676 1e−47 87 2586 1061 700741626H1 SOYMON012 g20728 BLASTN 676 1e−47 87 2587 1061 700789225H2 SOYMON011 g20728 BLASTN 339 1e−46 87 2588 1061 700548027H1 SOYMON001 g20728 BLASTN 368 1e−46 88 2589 1061 701070385H1 SOYMON034 g20728 BLASTN 370 1e−46 87 2590 1061 700681469H2 SOYMON008 g20728 BLASTN 411 1e−46 85 2591 1061 700548037H1 SOYMON001 g20728 BLASTN 526 1e−46 87 2592 1061 700646084H1 SOYMON011 g12158 BLASTN 564 1e−46 79 2593 1061 700752275H1 SOYMON014 g20728 BLASTN 629 1e−46 85 2594 1061 700683806H1 SOYMON008 g20728 BLASTN 660 1e−46 88 2595 1061 700654909H1 SOYMON004 g12158 BLASTN 666 1e−46 80 2596 1061 700986823H1 SOYMON009 g20728 BLASTN 667 1e−46 81 2597 1061 700741156H1 SOYMON012 g20728 BLASTN 304 1e−45 87 2598 1061 700906879H1 SOYMON022 g20728 BLASTN 398 1e−45 85 2599 1061 700875004H1 SOYMON018 g12158 BLASTN 647 1e−45 86 2600 1061 700996131H1 SOYMON018 g20728 BLASTN 648 1e−45 86 2601 1061 700873575H1 SOYMON018 g20728 BLASTN 648 1e−45 81 2602 1061 700990142H1 SOYMON011 g20728 BLASTN 648 1e−45 86 2603 1061 700981885H1 SOYMON009 g12158 BLASTN 651 1e−45 80 2604 1061 700874783H1 SOYMON018 g20728 BLASTN 653 1e−45 86 2605 1061 701110202H1 SOYMON036 g20728 BLASTN 656 1e−45 81 2606 1061 700683388H1 SOYMON008 g20728 BLASTN 640 1e−44 84 2607 1061 700875643H1 SOYMON018 g20728 BLASTN 643 1e−44 85 2608 1061 701001467H1 SOYMON018 g20728 BLASTN 414 1e−43 83 2609 1061 700787152H2 SOYMON011 g20728 BLASTN 428 1e−43 82 2610 1061 700683930H1 SOYMON008 g20728 BLASTN 339 1e−42 86 2611 1061 700740930H1 SOYMON012 g20728 BLASTN 367 1e−42 85 2612 1061 700787113H2 SOYMON011 g20728 BLASTN 394 1e−42 78 2613 1061 700739178H1 SOYMON012 g20728 BLASTN 415 1e−42 86 2614 1061 700986609H1 SOYMON009 g20728 BLASTN 529 1e−42 85 2615 1061 700683409H1 SOYMON008 g12158 BLASTN 582 1e−42 81 2616 1061 700743479H1 SOYMON012 g20728 BLASTN 545 1e−41 87 2617 1061 700681635H1 SOYMON008 g20728 BLASTN 553 1e−41 80 2618 1061 701109104H1 SOYMON036 g12158 BLASTN 596 1e−40 81 2619 1061 700871765H1 SOYMON018 g20728 BLASTN 578 1e−39 84 2620 1061 700992456H1 SOYMON011 g20728 BLASTN 403 1e−38 84 2621 1061 700554130H1 SOYMON001 g20728 BLASTN 563 1e−38 87 2622 1061 700742575H1 SOYMON012 g20728 BLASTN 564 1e−38 89 2623 1061 700875165H1 SOYMON018 g12158 BLASTN 568 1e−38 90 2624 1061 700686144H1 SOYMON008 g20728 BLASTN 569 1e−38 87 2625 1061 700990232H1 SOYMON011 g20728 BLASTN 572 1e−38 83 2626 1061 700657137H1 SOYMON004 g12158 BLASTN 574 1e−38 82 2627 1061 700731288H1 SOYMON009 g20728 BLASTN 339 1e−36 85 2628 1061 700741126H1 SOYMON012 g166703 BLASTN 465 1e−35 82 2629 1061 700975280H1 SOYMON009 g20728 BLASTN 517 1e−34 75 2630 1061 700788092H1 SOYMON011 g20728 BLASTN 264 1e−33 78 2631 1061 700683952H1 SOYMON008 g20728 BLASTN 364 1e−33 88 2632 1061 700992834H1 SOYMON011 g20728 BLASTN 380 1e−33 89 2633 1061 700991505H1 SOYMON011 g20728 BLASTN 460 1e−33 77 2634 1061 701110056H1 SOYMON036 g20728 BLASTN 490 1e−32 88 2635 1061 700679803H1 SOYMON007 g20728 BLASTN 490 1e−32 88 2636 1061 700686648H1 SOYMON008 g20728 BLASTN 483 1e−31 87 2637 1061 701000893H1 SOYMON018 g12158 BLASTN 253 1e−30 90 2638 1061 700729743H1 SOYMON009 g12158 BLASTN 362 1e−30 82 2639 1061 700656983H1 SOYMON004 g12158 BLASTN 379 1e−30 81 2640 1061 700742961H1 SOYMON012 g166701 BLASTN 469 1e−30 80 2641 1061 700995207H1 SOYMON011 g20728 BLASTN 322 1e−28 86 2642 1061 700960745H1 SOYMON022 g20728 BLASTN 444 1e−28 73 2643 1061 700873668H1 SOYMON018 g12158 BLASTN 337 1e−27 76 2644 1061 700991519H1 SOYMON011 g166701 BLASTN 435 1e−27 88 2645 1061 700743185H1 SOYMON012 g20728 BLASTN 427 1e−26 88 2646 1061 700554408H1 SOYMON001 g12158 BLASTN 221 1e−25 77 2647 1061 700686096H1 SOYMON008 g12158 BLASTN 326 1e−24 78 2648 1061 700739363H1 SOYMON012 g20728 BLASTN 401 1e−24 89 2649 1061 700996585H1 SOYMON018 g20728 BLASTN 416 1e−24 84 2650 1061 700991823H1 SOYMON011 g20728 BLASTN 422 1e−24 78 2651 1061 701000661H1 SOYMON018 g166702 BLASTX 130 1e−23 74 2652 1061 700606165H2 SOYMON008 g20728 BLASTN 389 1e−23 90 2653 1061 700999082H1 SOYMON018 g12158 BLASTN 364 1e−22 81 2654 1061 700738051H1 SOYMON012 g20728 BLASTN 376 1e−22 93 2655 1061 700740881H1 SOYMON012 g20728 BLASTN 377 1e−22 92 2656 1061 700987548H1 SOYMON009 g20728 BLASTN 347 1e−21 91 2657 1061 700739359H1 SOYMON012 g20728 BLASTN 357 1e−20 90 2658 1061 700979451H1 SOYMON009 g20728 BLASTN 357 1e−20 88 2659 1061 700991851H1 SOYMON011 g20728 BLASTN 351 1e−18 84 2660 1061 700989348H1 SOYMON011 g20728 BLASTN 295 1e−14 85 2661 1061 700558380H1 SOYMON001 g12159 BLASTX 80 1e−12 81 2662 1061 700738070H1 SOYMON012 g12158 BLASTN 160 1e−10 85 2663 1061 700992942H1 SOYMON011 g20728 BLASTN 243 1e−9 94 2664 1061 700986029H1 SOYMON009 g20728 BLASTN 208 1e−8 76 2665 1061 700743737H1 SOYMON012 g20728 BLASTN 231 1e−8 84 2666 12847 700680701H1 SOYMON008 g20732 BLASTN 547 1e−35 87 2667 12847 700874711H1 SOYMON018 g20732 BLASTN 486 1e−31 87 2668 1392 701051645H1 SOYMON032 g2078297 BLASTN 1065 1e−80 86 2669 1392 700563915H1 SOYMON002 g2078297 BLASTN 1072 1e−80 88 2670 1392 701204320H2 SOYMON035 g2078297 BLASTN 1005 1e−75 88 2671 1392 700652968H1 SOYMON003 g19565 BLASTN 1012 1e−75 83 2672 1392 700748683H1 SOYMON013 g169090 BLASTN 968 1e−71 86 2673 1392 700981771H1 SOYMON009 g2078297 BLASTN 552 1e−70 88 2674 1392 700605826H2 SOYMON006 g21142 BLASTN 618 1e−68 85 2675 1392 700666839H1 SOYMON005 g2078297 BLASTN 809 1e−68 88 2676 1392 700944037H1 SOYMON024 g19565 BLASTN 899 1e−66 83 2677 1392 700969575H1 SOYMON005 g19565 BLASTN 854 1e−62 83 2678 1392 701118935H1 SOYMON037 g19565 BLASTN 838 1e−61 83 2679 1392 700725758H1 SOYMON009 g19565 BLASTN 846 1e−61 81 2680 1392 701054027H1 SOYMON032 g19565 BLASTN 818 1e−59 83 2681 1392 700954591H1 SOYMON022 g19565 BLASTN 825 1e−59 83 2682 1392 700653724H1 SOYMON003 g19565 BLASTN 781 1e−56 83 2683 1392 701052969H1 SOYMON032 g19565 BLASTN 788 1e−56 82 2684 1392 700836192H1 SOYMON019 g19565 BLASTN 769 1e−55 84 2685 1392 701014006H1 SOYMON019 g19565 BLASTN 769 1e−55 84 2686 1392 700849014H1 SOYMON021 g19565 BLASTN 770 1e−55 83 2687 1392 700747177H1 SOYMON013 g19565 BLASTN 770 1e−55 83 2688 1392 700733933H1 SOYMON010 g19565 BLASTN 775 1e−55 83 2689 1392 701045883H1 SOYMON032 g19565 BLASTN 754 1e−54 83 2690 1392 700561161H1 SOYMON002 g19565 BLASTN 760 1e−54 83 2691 1392 701002757H2 SOYMON019 g19565 BLASTN 764 1e−54 84 2692 1392 701150827H1 SOYMON031 g21142 BLASTN 428 1e−53 88 2693 1392 701043855H1 SOYMON032 g19565 BLASTN 432 1e−53 84 2694 1392 701138753H1 SOYMON038 g166705 BLASTN 395 1e−52 80 2695 1392 700746913H1 SOYMON013 g19565 BLASTN 596 1e−52 84 2696 1392 701004953H1 SOYMON019 g19565 BLASTN 734 1e−52 83 2697 1392 700900882H1 SOYMON027 g19565 BLASTN 740 1e−52 83 2698 1392 700987148H1 SOYMON009 g19565 BLASTN 691 1e−51 83 2699 1392 701054872H1 SOYMON032 g19565 BLASTN 719 1e−51 81 2700 1392 701056763H1 SOYMON032 g166705 BLASTN 632 1e−50 83 2701 1392 700748607H1 SOYMON013 g19565 BLASTN 707 1e−50 82 2702 1392 700830473H1 SOYMON019 g19565 BLASTN 694 1e−49 83 2703 1392 700762033H1 SOYMON015 g19565 BLASTN 696 1e−49 82 2704 1392 700987949H1 SOYMON009 g19565 BLASTN 700 1e−49 83 2705 1392 701135194H1 SOYMON038 g19565 BLASTN 705 1e−49 82 2706 1392 700748676H1 SOYMON013 g19565 BLASTN 379 1e−48 83 2707 1392 701046095H1 SOYMON032 g166705 BLASTN 386 1e−48 83 2708 1392 701045383H1 SOYMON032 g21142 BLASTN 623 1e−48 82 2709 1392 701052575H1 SOYMON032 g19565 BLASTN 683 1e−48 83 2710 1392 700667935H1 SOYMON006 g19565 BLASTN 690 1e−48 82 2711 1392 701055287H1 SOYMON032 g19565 BLASTN 690 1e−48 80 2712 1392 700660946H1 SOYMON005 g19565 BLASTN 691 1e−48 82 2713 1392 700891889H1 SOYMON024 g19565 BLASTN 670 1e−47 82 2714 1392 700670279H1 SOYMON006 g19565 BLASTN 672 1e−47 83 2715 1392 700865105H1 SOYMON016 g21142 BLASTN 674 1e−47 82 2716 1392 700664974H1 SOYMON005 g19565 BLASTN 677 1e−47 83 2717 1392 700727084H1 SOYMON009 g19565 BLASTN 680 1e−47 82 2718 1392 700748807H1 SOYMON013 g19565 BLASTN 628 1e−46 80 2719 1392 700749971H1 SOYMON013 g21142 BLASTN 662 1e−46 81 2720 1392 700664177H1 SOYMON005 g19565 BLASTN 657 1e−45 83 2721 1392 700969206H1 SOYMON005 g166705 BLASTN 634 1e−44 84 2722 1392 700668696H1 SOYMON006 g19565 BLASTN 636 1e−44 83 2723 1392 700677777H1 SOYMON007 g19565 BLASTN 640 1e−44 83 2724 1392 700969506H1 SOYMON005 g21142 BLASTN 642 1e−44 81 2725 1392 700667829H1 SOYMON006 g166705 BLASTN 643 1e−44 82 2726 1392 700730321H1 SOYMON009 g166705 BLASTN 643 1e−44 82 2727 1392 700972412H1 SOYMON005 g166705 BLASTN 644 1e−44 82 2728 1392 701043160H1 SOYMON029 g21142 BLASTN 623 1e−43 84 2729 1392 700896562H1 SOYMON027 g21142 BLASTN 623 1e−43 84 2730 1392 700678284H1 SOYMON007 g21142 BLASTN 623 1e−43 84 2731 1392 700674379H1 SOYMON007 g21142 BLASTN 623 1e−43 84 2732 1392 700973321H1 SOYMON005 g21142 BLASTN 626 1e−43 82 2733 1392 700848568H1 SOYMON021 g166705 BLASTN 632 1e−43 84 2734 1392 700973272H1 SOYMON005 g19565 BLASTN 429 1e−42 83 2735 1392 700735988H1 SOYMON010 g21142 BLASTN 615 1e−42 80 2736 1392 701002533H1 SOYMON018 g19565 BLASTN 402 1e−41 83 2737 1392 700726201H1 SOYMON009 g19565 BLASTN 454 1e−41 81 2738 1392 701004758H1 SOYMON019 g166705 BLASTN 544 1e−41 83 2739 1392 701047055H1 SOYMON032 g166705 BLASTN 599 1e−41 85 2740 1392 700970781H1 SOYMON005 g166705 BLASTN 604 1e−41 83 2741 1392 700726274H1 SOYMON009 g19565 BLASTN 442 1e−40 82 2742 1392 701011762H1 SOYMON019 g166705 BLASTN 287 1e−39 79 2743 1392 700669086H1 SOYMON006 g21142 BLASTN 460 1e−39 83 2744 1392 700833089H1 SOYMON019 g166705 BLASTN 472 1e−39 82 2745 1392 700745795H1 SOYMON013 g19565 BLASTN 576 1e−39 76 2746 1392 700651350H1 SOYMON003 g166705 BLASTN 567 1e−38 83 2747 1392 700748761H1 SOYMON013 g166705 BLASTN 556 1e−37 83 2748 1392 701012075H1 SOYMON019 g166705 BLASTN 558 1e−37 84 2749 1392 700564585H1 SOYMON002 g21065 BLASTN 309 1e−36 85 2750 1392 701051053H1 SOYMON032 g166705 BLASTN 543 1e−36 84 2751 1392 700661104H1 SOYMON005 g166705 BLASTN 544 1e−35 85 2752 1392 701051845H1 SOYMON032 g19565 BLASTN 501 1e−32 84 2753 1392 700748992H1 SOYMON013 g21142 BLASTN 374 1e−22 82 2754 1392 700845656H1 SOYMON021 g166705 BLASTN 391 1e−22 83 2755 1392 700988562H1 SOYMON009 g1184773 BLASTN 397 1e−22 83 2756 1392 701003233H1 SOYMON019 g166705 BLASTN 249 1e−20 83 2757 1392 701048025H1 SOYMON032 g166705 BLASTN 335 1e−19 84 2758 14902 700977778H1 SOYMON009 g496493 BLASTN 1158 1e−87 90 2759 14902 700742004H1 SOYMON012 g496493 BLASTN 618 1e−81 90 2760 14902 700962586H1 SOYMON022 g496493 BLASTN 1023 1e−76 90 2761 14902 700994796H1 SOYMON011 g496493 BLASTN 480 1e−59 86 2762 16 700680820H1 SOYMON008 g169090 BLASTN 1392 1e−107 90 2763 16 700651027H1 SOYMON003 g169090 BLASTN 782 1e−101 87 2764 16 700661720H1 SOYMON005 g169090 BLASTN 1280 1e−98 84 2765 16 700653620H1 SOYMON003 g169090 BLASTN 783 1e−92 86 2766 16 701212010H1 SOYMON035 g169090 BLASTN 1193 1e−90 90 2767 16 700653624H1 SOYMON003 g169090 BLASTN 711 1e−86 86 2768 16 700684013H1 SOYMON008 g20732 BLASTN 1139 1e−86 89 2769 16 701130927H1 SOYMON038 g169090 BLASTN 1135 1e−85 90 2770 16 701118656H1 SOYMON037 g169090 BLASTN 927 1e−83 90 2771 16 701050807H1 SOYMON032 g169090 BLASTN 1101 1e−83 90 2772 16 700900304H1 SOYMON027 g169090 BLASTN 1108 1e−83 91 2773 16 700560856H1 SOYMON001 g20732 BLASTN 594 1e−82 88 2774 16 701127846H1 SOYMON037 g169090 BLASTN 1093 1e−82 90 2775 16 700746107H1 SOYMON013 g169090 BLASTN 1093 1e−82 91 2776 16 700957321H1 SOYMON022 g169090 BLASTN 1094 1e−82 90 2777 16 700556167H1 SOYMON001 g20732 BLASTN 1094 1e−82 87 2778 16 700685605H1 SOYMON008 g20732 BLASTN 1095 1e−82 89 2779 16 700982024H1 SOYMON009 g169090 BLASTN 1097 1e−82 87 2780 16 701136318H1 SOYMON038 g169090 BLASTN 912 1e−81 90 2781 16 701045985H1 SOYMON032 g169090 BLASTN 1083 1e−81 91 2782 16 700896756H1 SOYMON027 g169090 BLASTN 1083 1e−81 89 2783 16 700738664H1 SOYMON012 g20732 BLASTN 1087 1e−81 89 2784 16 700982290H1 SOYMON009 g169090 BLASTN 1088 1e−81 88 2785 16 701039411H1 SOYMON029 g169090 BLASTN 1068 1e−80 88 2786 16 700760151H1 SOYMON015 g169090 BLASTN 1076 1e−80 87 2787 16 701037105H1 SOYMON029 g169090 BLASTN 706 1e−79 90 2788 16 700653646H1 SOYMON003 g169090 BLASTN 723 1e−79 83 2789 16 701003361H1 SOYMON019 g169090 BLASTN 913 1e−79 88 2790 16 700684871H1 SOYMON008 g169090 BLASTN 1058 1e−79 90 2791 16 700972333H1 SOYMON005 g169090 BLASTN 1059 1e−79 89 2792 16 700660117H1 SOYMON004 g20732 BLASTN 1060 1e−79 91 2793 16 700681841H1 SOYMON008 g169090 BLASTN 1060 1e−79 89 2794 16 701063487H1 SOYMON033 g169090 BLASTN 1063 1e−79 87 2795 16 701118518H1 SOYMON037 g169090 BLASTN 1064 1e−79 92 2796 16 700998228H1 SOYMON018 g169090 BLASTN 599 1e−78 91 2797 16 700667222H1 SOYMON006 g169090 BLASTN 1042 1e−78 87 2798 16 701205378H1 SOYMON035 g169090 BLASTN 1047 1e−78 89 2799 16 701109009H1 SOYMON036 g169090 BLASTN 1050 1e−78 85 2800 16 700902080H1 SOYMON027 g20732 BLASTN 1051 1e−78 88 2801 16 701065402H1 SOYMON034 g20732 BLASTN 1051 1e−78 85 2802 16 700905151H1 SOYMON022 g169090 BLASTN 1052 1e−78 89 2803 16 700660104H1 SOYMON004 g20732 BLASTN 1053 1e−78 91 2804 16 701122747H1 SOYMON037 g169090 BLASTN 1029 1e−77 85 2805 16 700681958H1 SOYMON008 g20732 BLASTN 1033 1e−77 87 2806 16 701045633H1 SOYMON032 g169090 BLASTN 1036 1e−77 86 2807 16 700870706H1 SOYMON018 g169090 BLASTN 1038 1e−77 89 2808 16 700957310H1 SOYMON022 g169090 BLASTN 1040 1e−77 91 2809 16 700981914H1 SOYMON009 g169090 BLASTN 455 1e−76 83 2810 16 700873416H1 SOYMON018 g20732 BLASTN 544 1e−76 88 2811 16 700562964H1 SOYMON002 g169090 BLASTN 824 1e−76 88 2812 16 700829678H1 SOYMON019 g169090 BLASTN 1021 1e−76 88 2813 16 700668218H1 SOYMON006 g20732 BLASTN 1023 1e−76 87 2814 16 701206845H1 SOYMON035 g169090 BLASTN 1024 1e−76 90 2815 16 700835082H1 SOYMON019 g169090 BLASTN 1024 1e−76 88 2816 16 701011483H1 SOYMON019 g169090 BLASTN 1024 1e−76 90 2817 16 700605436H2 SOYMON004 g20732 BLASTN 1027 1e−76 86 2818 16 700963428H1 SOYMON022 g20732 BLASTN 1027 1e−76 89 2819 16 700975672H1 SOYMON009 g20732 BLASTN 852 1e−75 90 2820 16 700907957H1 SOYMON022 g169090 BLASTN 1005 1e−75 91 2821 16 700960608H1 SOYMON022 g169090 BLASTN 1005 1e−75 88 2822 16 700837794H1 SOYMON020 g169090 BLASTN 1006 1e−75 91 2823 16 701138460H1 SOYMON038 g169090 BLASTN 1006 1e−75 88 2824 16 700646202H1 SOYMON012 g20732 BLASTN 1007 1e−75 88 2825 16 700874447H1 SOYMON018 g20732 BLASTN 1007 1e−75 90 2826 16 700667967H1 SOYMON006 g20732 BLASTN 1007 1e−75 89 2827 16 701131790H1 SOYMON038 g169090 BLASTN 1011 1e−75 91 2828 16 700970954H1 SOYMON005 g169090 BLASTN 1012 1e−75 87 2829 16 701120441H1 SOYMON037 g169090 BLASTN 1013 1e−75 87 2830 16 701120055H1 SOYMON037 g169090 BLASTN 1015 1e−75 83 2831 16 701001031H1 SOYMON018 g20732 BLASTN 1017 1e−75 83 2832 16 700652931H1 SOYMON003 g169090 BLASTN 853 1e−74 79 2833 16 700981202H1 SOYMON009 g169090 BLASTN 955 1e−74 87 2834 16 701142183H1 SOYMON038 g169090 BLASTN 1000 1e−74 85 2835 16 700978682H1 SOYMON009 g169090 BLASTN 1000 1e−74 85 2836 16 701122065H1 SOYMON037 g169090 BLASTN 1004 1e−74 87 2837 16 700558895H1 SOYMON001 g20732 BLASTN 566 1e−73 86 2838 16 700686234H1 SOYMON008 g20732 BLASTN 573 1e−73 89 2839 16 700566271H1 SOYMON002 g169090 BLASTN 863 1e−73 84 2840 16 700558604H1 SOYMON001 g20732 BLASTN 982 1e−73 82 2841 16 700684166H1 SOYMON008 g169090 BLASTN 984 1e−73 86 2842 16 700873924H1 SOYMON018 g169090 BLASTN 986 1e−73 88 2843 16 700738880H1 SOYMON012 g20732 BLASTN 987 1e−73 89 2844 16 700741816H1 SOYMON012 g20732 BLASTN 992 1e−73 86 2845 16 700892371H1 SOYMON024 g169090 BLASTN 992 1e−73 88 2846 16 700560702H1 SOYMON001 g20732 BLASTN 993 1e−73 82 2847 16 700968331H1 SOYMON036 g20732 BLASTN 993 1e−73 88 2848 16 701063318H1 SOYMON033 g169090 BLASTN 787 1e−72 88 2849 16 700996472H1 SOYMON018 g20732 BLASTN 821 1e−72 86 2850 16 701065057H1 SOYMON034 g169090 BLASTN 924 1e−72 84 2851 16 700863670H1 SOYMON027 g169090 BLASTN 943 1e−72 90 2852 16 701212013H1 SOYMON035 g169090 BLASTN 969 1e−72 85 2853 16 701012801H1 SOYMON019 g169090 BLASTN 969 1e−72 85 2854 16 701004406H1 SOYMON019 g169090 BLASTN 969 1e−72 85 2855 16 700751116H1 SOYMON014 g169090 BLASTN 970 1e−72 90 2856 16 700675491H1 SOYMON007 g169090 BLASTN 972 1e−72 92 2857 16 701131360H1 SOYMON038 g169090 BLASTN 972 1e−72 84 2858 16 700562740H1 SOYMON002 g169090 BLASTN 976 1e−72 83 2859 16 701099556H1 SOYMON028 g169090 BLASTN 979 1e−72 88 2860 16 700558534H1 SOYMON001 g20732 BLASTN 469 1e−71 84 2861 16 700565245H1 SOYMON002 g169090 BLASTN 715 1e−71 90 2862 16 700944452H1 SOYMON024 g169090 BLASTN 780 1e−71 86 2863 16 701009629H1 SOYMON019 g169090 BLASTN 828 1e−71 84 2864 16 700725661H1 SOYMON009 g169090 BLASTN 838 1e−71 87 2865 16 701066885H1 SOYMON034 g169090 BLASTN 856 1e−71 86 2866 16 701009856H1 SOYMON019 g169090 BLASTN 958 1e−71 83 2867 16 700560569H1 SOYMON001 g169090 BLASTN 963 1e−71 84 2868 16 700867802H1 SOYMON016 g169090 BLASTN 964 1e−71 85 2869 16 701117421H1 SOYMON037 g169090 BLASTN 967 1e−71 83 2870 16 700963317H1 SOYMON022 g20732 BLASTN 830 1e−70 85 2871 16 700646149H1 SOYMON012 g20732 BLASTN 864 1e−70 87 2872 16 701002213H1 SOYMON018 g20732 BLASTN 946 1e−70 88 2873 16 700999509H1 SOYMON018 g20732 BLASTN 948 1e−70 83 2874 16 701003210H1 SOYMON019 g169090 BLASTN 949 1e−70 83 2875 16 700738832H1 SOYMON012 g20732 BLASTN 952 1e−70 86 2876 16 701212329H1 SOYMON035 g169090 BLASTN 952 1e−70 85 2877 16 700683783H1 SOYMON008 g169090 BLASTN 953 1e−70 83 2878 16 700874828H1 SOYMON018 g20732 BLASTN 953 1e−70 85 2879 16 700839986H1 SOYMON020 g169090 BLASTN 954 1e−70 89 2880 16 700661155H1 SOYMON005 g169090 BLASTN 955 1e−70 84 2881 16 700686453H1 SOYMON008 g20732 BLASTN 956 1e−70 85 2882 16 701104636H1 SOYMON036 g169090 BLASTN 956 1e−70 84 2883 16 700682277H1 SOYMON008 g20732 BLASTN 444 1e−69 88 2884 16 700556648H1 SOYMON001 g20732 BLASTN 526 1e−69 83 2885 16 701133126H1 SOYMON038 g169090 BLASTN 526 1e−69 86 2886 16 700659056H1 SOYMON004 g169090 BLASTN 655 1e−69 91 2887 16 701009405H1 SOYMON019 g169090 BLASTN 665 1e−69 91 2888 16 700554721H1 SOYMON001 g169090 BLASTN 743 1e−69 81 2889 16 700833925H1 SOYMON019 g169090 BLASTN 938 1e−69 85 2890 16 700848119H1 SOYMON021 g20550 BLASTN 942 1e−69 85 2891 16 700559336H1 SOYMON001 g169090 BLASTN 943 1e−69 80 2892 16 701207095H1 SOYMON035 g169090 BLASTN 944 1e−69 83 2893 16 701125617H1 SOYMON037 g169090 BLASTN 944 1e−69 84 2894 16 700756418H1 SOYMON014 g169090 BLASTN 944 1e−69 84 2895 16 700738263H1 SOYMON012 g20732 BLASTN 945 1e−69 89 2896 16 700743026H1 SOYMON012 g169090 BLASTN 497 1e−68 85 2897 16 700978803H1 SOYMON009 g169090 BLASTN 931 1e−68 80 2898 16 700852390H1 SOYMON023 g20732 BLASTN 489 1e−67 87 2899 16 700681390H2 SOYMON008 g20732 BLASTN 506 1e−67 88 2900 16 700554330H1 SOYMON001 g20732 BLASTN 794 1e−67 83 2901 16 700746738H1 SOYMON013 g169090 BLASTN 910 1e−67 86 2902 16 700962884H1 SOYMON022 g169090 BLASTN 919 1e−67 85 2903 16 700683756H1 SOYMON008 g20732 BLASTN 919 1e−67 83 2904 16 700898676H1 SOYMON027 g169090 BLASTN 919 1e−67 91 2905 16 700685076H1 SOYMON008 g20732 BLASTN 921 1e−67 85 2906 16 700836262H1 SOYMON019 g169090 BLASTN 898 1e−66 84 2907 16 700674865H1 SOYMON007 g169090 BLASTN 902 1e−66 90 2908 16 700967318H1 SOYMON031 g20732 BLASTN 906 1e−66 85 2909 16 700955044H1 SOYMON022 g169090 BLASTN 907 1e−66 85 2910 16 700755131H1 SOYMON014 g20732 BLASTN 908 1e−66 85 2911 16 700743643H1 SOYMON012 g20732 BLASTN 909 1e−66 84 2912 16 700979861H2 SOYMON009 g169090 BLASTN 293 1e−65 88 2913 16 700907981H1 SOYMON022 g20550 BLASTN 681 1e−65 85 2914 16 701001058H1 SOYMON018 g20732 BLASTN 690 1e−65 81 2915 16 700547949H1 SOYMON001 g20732 BLASTN 835 1e−65 88 2916 16 700678780H1 SOYMON007 g169090 BLASTN 854 1e−65 92 2917 16 700851960H1 SOYMON023 g20550 BLASTN 890 1e−65 85 2918 16 701099668H1 SOYMON028 g169090 BLASTN 493 1e−64 83 2919 16 701103733H1 SOYMON036 g169090 BLASTN 684 1e−64 80 2920 16 700985604H1 SOYMON009 g169090 BLASTN 873 1e−64 79 2921 16 700849622H1 SOYMON021 g169090 BLASTN 877 1e−64 84 2922 16 700752648H1 SOYMON014 g169090 BLASTN 879 1e−64 85 2923 16 700952882H1 SOYMON022 g20732 BLASTN 884 1e−64 85 2924 16 701006721H1 SOYMON019 g169090 BLASTN 884 1e−64 86 2925 16 700895879H1 SOYMON027 g169090 BLASTN 884 1e−64 84 2926 16 700740632H1 SOYMON012 g20732 BLASTN 375 1e−63 84 2927 16 700981723H1 SOYMON009 g20732 BLASTN 690 1e−63 81 2928 16 700657114H1 SOYMON004 g169090 BLASTN 861 1e−63 87 2929 16 700661319H1 SOYMON005 g169090 BLASTN 862 1e−63 82 2930 16 700987848H1 SOYMON009 g169090 BLASTN 862 1e−63 79 2931 16 700664376H1 SOYMON005 g169090 BLASTN 865 1e−63 83 2932 16 700848760H1 SOYMON021 g169090 BLASTN 868 1e−63 82 2933 16 700734932H1 SOYMON010 g169090 BLASTN 871 1e−63 90 2934 16 700894550H1 SOYMON024 g169090 BLASTN 872 1e−63 86 2935 16 700754237H1 SOYMON014 g169090 BLASTN 443 1e−62 83 2936 16 700654194H1 SOYMON003 g169090 BLASTN 449 1e−62 83 2937 16 701002119H1 SOYMON018 g20732 BLASTN 459 1e−62 89 2938 16 700899445H1 SOYMON027 g20732 BLASTN 473 1e−62 86 2939 16 700648324H1 SOYMON003 g169090 BLASTN 531 1e−62 80 2940 16 700897837H1 SOYMON027 g169090 BLASTN 582 1e−62 82 2941 16 701056234H1 SOYMON032 g169090 BLASTN 737 1e−62 79 2942 16 700906196H1 SOYMON022 g169090 BLASTN 852 1e−62 83 2943 16 701002126H1 SOYMON018 g20732 BLASTN 853 1e−62 82 2944 16 700853304H1 SOYMON023 g169090 BLASTN 857 1e−62 84 2945 16 701015618H1 SOYMON037 g169090 BLASTN 857 1e−62 81 2946 16 700875928H1 SOYMON018 g20732 BLASTN 861 1e−62 86 2947 16 700676860H1 SOYMON007 g169090 BLASTN 461 1e−61 84 2948 16 700983517H1 SOYMON009 g409574 BLASTN 615 1e−61 86 2949 16 700841881H1 SOYMON020 g20550 BLASTN 717 1e−61 86 2950 16 700853082H1 SOYMON023 g169090 BLASTN 842 1e−61 84 2951 16 701106263H1 SOYMON036 g20732 BLASTN 844 1e−61 90 2952 16 700678241H1 SOYMON007 g169090 BLASTN 845 1e−61 83 2953 16 701133107H1 SOYMON038 g169090 BLASTN 845 1e−61 79 2954 16 700976170H1 SOYMON009 g169090 BLASTN 848 1e−61 78 2955 16 700646259H1 SOYMON012 g20732 BLASTN 650 1e−60 82 2956 16 700682750H1 SOYMON008 g169090 BLASTN 654 1e−60 83 2957 16 700556141H1 SOYMON001 g20732 BLASTN 690 1e−60 81 2958 16 700870652H1 SOYMON018 g20732 BLASTN 702 1e−60 86 2959 16 700893834H1 SOYMON024 g169090 BLASTN 826 1e−60 82 2960 16 700970819H1 SOYMON005 g169090 BLASTN 828 1e−60 81 2961 16 700890650H1 SOYMON024 g169090 BLASTN 830 1e−60 88 2962 16 701122211H1 SOYMON037 g169090 BLASTN 830 1e−60 83 2963 16 700980742H1 SOYMON009 g169090 BLASTN 830 1e−60 84 2964 16 701137606H1 SOYMON038 g169090 BLASTN 832 1e−60 83 2965 16 700682612H2 SOYMON008 g20732 BLASTN 834 1e−60 81 2966 16 700971830H1 SOYMON005 g169090 BLASTN 835 1e−60 79 2967 16 700909405H1 SOYMON022 g169090 BLASTN 835 1e−60 79 2968 16 700981291H1 SOYMON009 g169090 BLASTN 835 1e−60 79 2969 16 700953564H1 SOYMON022 g169090 BLASTN 836 1e−60 82 2970 16 700747612H1 SOYMON013 g409574 BLASTN 836 1e−60 83 2971 16 700975021H1 SOYMON005 g169090 BLASTN 439 1e−59 82 2972 16 700729321H1 SOYMON009 g309670 BLASTN 485 1e−59 81 2973 16 701001137H1 SOYMON018 g20732 BLASTN 578 1e−59 79 2974 16 700554280H1 SOYMON001 g20732 BLASTN 596 1e−59 88 2975 16 701135387H1 SOYMON038 g169090 BLASTN 609 1e−59 80 2976 16 700655905H1 SOYMON004 g169090 BLASTN 646 1e−59 82 2977 16 701048613H1 SOYMON032 g169090 BLASTN 814 1e−59 79 2978 16 701062603H1 SOYMON033 g166705 BLASTN 814 1e−59 83 2979 16 700741884H1 SOYMON012 g169090 BLASTN 815 1e−59 83 2980 16 701014048H1 SOYMON019 g169090 BLASTN 815 1e−59 84 2981 16 700556774H1 SOYMON001 g20732 BLASTN 817 1e−59 82 2982 16 701212143H1 SOYMON035 g169090 BLASTN 819 1e−59 79 2983 16 700977724H1 SOYMON009 g169090 BLASTN 819 1e−59 83 2984 16 701052505H1 SOYMON032 g169090 BLASTN 821 1e−59 84 2985 16 701048090H1 SOYMON032 g169090 BLASTN 823 1e−59 85 2986 16 700850111H1 SOYMON023 g169090 BLASTN 802 1e−58 80 2987 16 700748768H1 SOYMON013 g169090 BLASTN 804 1e−58 85 2988 16 701215404H1 SOYMON035 g169090 BLASTN 806 1e−58 84 2989 16 700686206H1 SOYMON008 g20732 BLASTN 807 1e−58 82 2990 16 701137704H1 SOYMON038 g409574 BLASTN 808 1e−58 82 2991 16 700876594H1 SOYMON018 g169090 BLASTN 809 1e−58 83 2992 16 700743816H1 SOYMON012 g20732 BLASTN 809 1e−58 90 2993 16 701037342H1 SOYMON029 g409574 BLASTN 812 1e−58 82 2994 16 700853152H1 SOYMON023 g169090 BLASTN 576 1e−57 87 2995 16 700905876H1 SOYMON022 g169090 BLASTN 606 1e−57 84 2996 16 700790719H1 SOYMON011 g409574 BLASTN 710 1e−57 82 2997 16 701106994H1 SOYMON036 g169090 BLASTN 790 1e−57 79 2998 16 700752366H1 SOYMON014 g169090 BLASTN 790 1e−57 81 2999 16 700952951H1 SOYMON022 g169090 BLASTN 791 1e−57 84 3000 16 700998563H1 SOYMON018 g20732 BLASTN 792 1e−57 88 3001 16 700840245H1 SOYMON020 g169090 BLASTN 792 1e−57 79 3002 16 700556140H1 SOYMON001 g166705 BLASTN 794 1e−57 82 3003 16 701056981H1 SOYMON033 g169090 BLASTN 795 1e−57 83 3004 16 700953045H1 SOYMON022 g169090 BLASTN 796 1e−57 83 3005 16 701137408H1 SOYMON038 g169090 BLASTN 797 1e−57 82 3006 16 700972258H1 SOYMON005 g169090 BLASTN 797 1e−57 79 3007 16 700980774H1 SOYMON009 g169090 BLASTN 797 1e−57 88 3008 16 700972064H1 SOYMON005 g169090 BLASTN 797 1e−57 79 3009 16 700685812H1 SOYMON008 g169090 BLASTN 798 1e−57 79 3010 16 700740477H1 SOYMON012 g409574 BLASTN 801 1e−57 84 3011 16 701062012H1 SOYMON033 g409574 BLASTN 451 1e−56 82 3012 16 701108736H1 SOYMON036 g20732 BLASTN 529 1e−56 80 3013 16 701104521H1 SOYMON036 g169090 BLASTN 680 1e−56 84 3014 16 700659833H1 SOYMON004 g2905771 BLASTN 754 1e−56 97 3015 16 700786076H2 SOYMON011 g2905771 BLASTN 754 1e−56 97 3016 16 700666231H1 SOYMON005 g2905771 BLASTN 754 1e−56 97 3017 16 700556330H1 SOYMON001 g20732 BLASTN 779 1e−56 81 3018 16 700964614H1 SOYMON022 g19565 BLASTN 780 1e−56 84 3019 16 700985844H1 SOYMON009 g19565 BLASTN 780 1e−56 84 3020 16 701126134H1 SOYMON037 g409574 BLASTN 781 1e−56 83 3021 16 700968036H1 SOYMON034 g169090 BLASTN 786 1e−56 85 3022 16 701110182H1 SOYMON036 g169090 BLASTN 786 1e−56 85 3023 16 700995174H1 SOYMON011 g169090 BLASTN 787 1e−56 85 3024 16 701044955H1 SOYMON032 g2905771 BLASTN 404 1e−55 96 3025 16 701203714H2 SOYMON035 g2905771 BLASTN 413 1e−55 97 3026 16 700847062H1 SOYMON021 g169090 BLASTN 528 1e−55 83 3027 16 700876923H1 SOYMON018 g20732 BLASTN 568 1e−55 81 3028 16 700738183H1 SOYMON012 g20732 BLASTN 586 1e−55 81 3029 16 701001383H1 SOYMON018 g20732 BLASTN 590 1e−55 81 3030 16 700877113H1 SOYMON018 g20732 BLASTN 681 1e−55 80 3031 16 700562672H1 SOYMON002 g169090 BLASTN 693 1e−55 83 3032 16 700956242H1 SOYMON022 g2905771 BLASTN 740 1e−55 96 3033 16 701058012H1 SOYMON033 g2905771 BLASTN 747 1e−55 96 3034 16 701070207H1 SOYMON034 g2905771 BLASTN 747 1e−55 96 3035 16 700901724H1 SOYMON027 g2905771 BLASTN 747 1e−55 96 3036 16 700792920H1 SOYMON017 g169090 BLASTN 767 1e−55 83 3037 16 700964732H1 SOYMON022 g169090 BLASTN 768 1e−55 84 3038 16 700994809H1 SOYMON011 g409574 BLASTN 768 1e−55 83 3039 16 700987118H1 SOYMON009 g19565 BLASTN 769 1e−55 84 3040 16 701007268H2 SOYMON019 g169090 BLASTN 769 1e−55 83 3041 16 700650971H1 SOYMON003 g169090 BLASTN 770 1e−55 91 3042 16 700964742H1 SOYMON022 g169090 BLASTN 771 1e−55 85 3043 16 700662524H1 SOYMON005 g169090 BLASTN 772 1e−55 79 3044 16 700895349H1 SOYMON027 g20732 BLASTN 772 1e−55 89 3045 16 701008593H1 SOYMON019 g169090 BLASTN 776 1e−55 82 3046 16 701004062H1 SOYMON019 g169090 BLASTN 326 1e−54 81 3047 16 700731710H1 SOYMON010 g169090 BLASTN 456 1e−54 84 3048 16 700742019H1 SOYMON012 g409574 BLASTN 483 1e−54 83 3049 16 700944396H1 SOYMON024 g169090 BLASTN 610 1e−54 84 3050 16 701139717H1 SOYMON038 g169090 BLASTN 639 1e−54 81 3051 16 700555467H1 SOYMON001 g20732 BLASTN 688 1e−54 81 3052 16 701041622H1 SOYMON029 g2905771 BLASTN 738 1e−54 96 3053 16 700736350H1 SOYMON010 g409574 BLASTN 754 1e−54 83 3054 16 700996720H1 SOYMON018 g409574 BLASTN 755 1e−54 82 3055 16 700987832H1 SOYMON009 g169090 BLASTN 759 1e−54 79 3056 16 700841935H1 SOYMON020 g20732 BLASTN 763 1e−54 81 3057 16 700808443H1 SOYMON024 g169090 BLASTN 765 1e−54 84 3058 16 700959733H1 SOYMON022 g409574 BLASTN 435 1e−53 81 3059 16 700646537H1 SOYMON014 g169090 BLASTN 445 1e−53 85 3060 16 701006244H2 SOYMON019 g169090 BLASTN 541 1e−53 85 3061 16 701059852H1 SOYMON033 g2905771 BLASTN 661 1e−53 92 3062 16 700876815H1 SOYMON018 g169090 BLASTN 668 1e−53 81 3063 16 700749752H1 SOYMON013 g19565 BLASTN 742 1e−53 84 3064 16 700736445H1 SOYMON010 g169090 BLASTN 746 1e−53 84 3065 16 700990431H1 SOYMON011 g20732 BLASTN 747 1e−53 86 3066 16 700990414H1 SOYMON011 g20732 BLASTN 749 1e−53 86 3067 16 700740171H1 SOYMON012 g169090 BLASTN 749 1e−53 83 3068 16 700875936H1 SOYMON018 g20732 BLASTN 400 1e−52 84 3069 16 701132471H1 SOYMON038 g409574 BLASTN 479 1e−52 82 3070 16 701064163H1 SOYMON034 g169090 BLASTN 519 1e−52 85 3071 16 701120529H1 SOYMON037 g169090 BLASTN 602 1e−52 80 3072 16 700787014H2 SOYMON011 g169090 BLASTN 622 1e−52 84 3073 16 701214833H1 SOYMON035 g169090 BLASTN 677 1e−52 82 3074 16 700741593H1 SOYMON012 g409574 BLASTN 707 1e−52 83 3075 16 700792328H1 SOYMON017 g2905771 BLASTN 715 1e−52 100 3076 16 700838427H1 SOYMON020 g169090 BLASTN 730 1e−52 79 3077 16 700985453H1 SOYMON009 g169090 BLASTN 731 1e−52 84 3078 16 700732002H1 SOYMON010 g169090 BLASTN 732 1e−52 77 3079 16 700906172H1 SOYMON022 g169090 BLASTN 732 1e−52 79 3080 16 701137118H1 SOYMON038 g19565 BLASTN 734 1e−52 84 3081 16 701013823H1 SOYMON019 g169090 BLASTN 736 1e−52 84 3082 16 700686616H1 SOYMON008 g309670 BLASTN 736 1e−52 88 3083 16 700962944H1 SOYMON022 g169090 BLASTN 737 1e−52 79 3084 16 700945903H1 SOYMON024 g169090 BLASTN 737 1e−52 79 3085 16 700863880H1 SOYMON016 g169090 BLASTN 737 1e−52 79 3086 16 700754937H1 SOYMON014 g169090 BLASTN 737 1e−52 79 3087 16 701059066H1 SOYMON033 g169090 BLASTN 737 1e−52 79 3088 16 700757083H1 SOYMON015 g169090 BLASTN 737 1e−52 81 3089 16 701043292H1 SOYMON029 g409574 BLASTN 739 1e−52 83 3090 16 700839971H1 SOYMON020 g169090 BLASTN 740 1e−52 78 3091 16 700897536H1 SOYMON027 g20732 BLASTN 740 1e−52 85 3092 16 700748758H1 SOYMON013 g169090 BLASTN 741 1e−52 80 3093 16 700737167H1 SOYMON010 g20550 BLASTN 474 1e−51 83 3094 16 700792472H1 SOYMON017 g409574 BLASTN 489 1e−51 84 3095 16 701002831H1 SOYMON019 g409574 BLASTN 495 1e−51 83 3096 16 701147120H1 SOYMON031 g169090 BLASTN 592 1e−51 86 3097 16 700993103H1 SOYMON011 g409574 BLASTN 679 1e−51 81 3098 16 700681212H1 SOYMON008 g20732 BLASTN 684 1e−51 82 3099 16 700787050H2 SOYMON011 g20732 BLASTN 722 1e−51 82 3100 16 700964087H1 SOYMON022 g169090 BLASTN 723 1e−51 83 3101 16 701131690H1 SOYMON038 g169090 BLASTN 724 1e−51 80 3102 16 701013216H1 SOYMON019 g169090 BLASTN 724 1e−51 84 3103 16 700752307H1 SOYMON014 g169090 BLASTN 727 1e−51 79 3104 16 700963986H1 SOYMON022 g169090 BLASTN 727 1e−51 79 3105 16 700945596H1 SOYMON024 g19565 BLASTN 728 1e−51 83 3106 16 700786782H2 SOYMON011 g169090 BLASTN 728 1e−51 79 3107 16 700686279H1 SOYMON008 g20732 BLASTN 415 1e−50 82 3108 16 700558939H1 SOYMON001 g20732 BLASTN 472 1e−50 78 3109 16 701118441H1 SOYMON037 g169090 BLASTN 495 1e−50 80 3110 16 701046150H1 SOYMON032 g169090 BLASTN 605 1e−50 83 3111 16 700876929H1 SOYMON018 g20732 BLASTN 681 1e−50 82 3112 16 700945352H1 SOYMON024 g2905771 BLASTN 685 1e−50 91 3113 16 700725046H1 SOYMON009 g2905771 BLASTN 688 1e−50 94 3114 16 700869271H1 SOYMON016 g2905771 BLASTN 688 1e−50 94 3115 16 700841465H1 SOYMON020 g19565 BLASTN 707 1e−50 83 3116 16 701213349H1 SOYMON035 g169090 BLASTN 712 1e−50 85 3117 16 700726069H1 SOYMON009 g19565 BLASTN 712 1e−50 84 3118 16 701055733H1 SOYMON032 g19565 BLASTN 712 1e−50 84 3119 16 700663235H1 SOYMON005 g169090 BLASTN 712 1e−50 79 3120 16 700963289H1 SOYMON022 g169090 BLASTN 712 1e−50 85 3121 16 700686557H1 SOYMON008 g169090 BLASTN 712 1e−50 85 3122 16 701127887H1 SOYMON037 g169090 BLASTN 713 1e−50 80 3123 16 700833351H1 SOYMON019 g169090 BLASTN 717 1e−50 85 3124 16 700975879H1 SOYMON009 g167043 BLASTN 379 1e−49 82 3125 16 700731970H1 SOYMON010 g2905771 BLASTN 675 1e−49 100 3126 16 700750149H1 SOYMON013 g169090 BLASTN 695 1e−49 85 3127 16 700953068H1 SOYMON022 g169090 BLASTN 696 1e−49 79 3128 16 700847286H1 SOYMON021 g19565 BLASTN 696 1e−49 82 3129 16 701043647H1 SOYMON029 g19565 BLASTN 696 1e−49 82 3130 16 700985440H1 SOYMON009 g169090 BLASTN 698 1e−49 84 3131 16 701204172H1 SOYMON035 g169090 BLASTN 698 1e−49 84 3132 16 700944204H1 SOYMON024 g169090 BLASTN 701 1e−49 79 3133 16 700906132H1 SOYMON022 g169090 BLASTN 702 1e−49 85 3134 16 701145287H1 SOYMON031 g19565 BLASTN 702 1e−49 83 3135 16 700748555H1 SOYMON013 g19565 BLASTN 703 1e−49 83 3136 16 700791357H1 SOYMON011 g169090 BLASTN 704 1e−49 85 3137 16 701132090H1 SOYMON038 g409574 BLASTN 704 1e−49 83 3138 16 700998663H1 SOYMON018 g20732 BLASTN 705 1e−49 78 3139 16 701060890H1 SOYMON033 g2078297 BLASTN 429 1e−48 81 3140 16 700986781H1 SOYMON009 g166705 BLASTN 453 1e−48 83 3141 16 700953335H1 SOYMON022 g19565 BLASTN 623 1e−48 84 3142 16 701014706H1 SOYMON019 g19565 BLASTN 644 1e−48 85 3143 16 701119782H1 SOYMON037 g2905771 BLASTN 658 1e−48 92 3144 16 701108783H1 SOYMON036 g2905771 BLASTN 664 1e−48 97 3145 16 700866439H1 SOYMON016 g169090 BLASTN 682 1e−48 77 3146 16 700762316H1 SOYMON015 g169090 BLASTN 682 1e−48 83 3147 16 700901056H1 SOYMON027 g169090 BLASTN 686 1e−48 79 3148 16 701104412H1 SOYMON036 g20732 BLASTN 690 1e−48 79 3149 16 700738192H1 SOYMON012 g20732 BLASTN 690 1e−48 79 3150 16 700752442H1 SOYMON014 g20732 BLASTN 690 1e−48 79 3151 16 700740385H1 SOYMON012 g20732 BLASTN 690 1e−48 79 3152 16 701137084H1 SOYMON038 g169090 BLASTN 691 1e−48 84 3153 16 701010003H2 SOYMON019 g169090 BLASTN 692 1e−48 85 3154 16 700833047H1 SOYMON019 g169090 BLASTN 546 1e−47 86 3155 16 700855933H1 SOYMON023 g169090 BLASTN 550 1e−47 85 3156 16 701014245H1 SOYMON019 g19565 BLASTN 581 1e−47 84 3157 16 700762962H1 SOYMON015 g169090 BLASTN 604 1e−47 86 3158 16 700975559H1 SOYMON009 g2905771 BLASTN 645 1e−47 100 3159 16 701151663H1 SOYMON031 g169090 BLASTN 671 1e−47 85 3160 16 700840645H1 SOYMON020 g169090 BLASTN 672 1e−47 80 3161 16 700787505H1 SOYMON011 g20732 BLASTN 674 1e−47 80 3162 16 700672894H1 SOYMON006 g169090 BLASTN 675 1e−47 83 3163 16 700678041H1 SOYMON007 g20732 BLASTN 677 1e−47 80 3164 16 701205624H1 SOYMON035 g409574 BLASTN 680 1e−47 82 3165 16 701044525H1 SOYMON032 g169090 BLASTN 681 1e−47 90 3166 16 700998789H1 SOYMON018 g169090 BLASTN 681 1e−47 78 3167 16 700997577H1 SOYMON018 g20732 BLASTN 681 1e−47 79 3168 16 700849115H1 SOYMON021 g2905771 BLASTN 350 1e−46 95 3169 16 700660742H1 SOYMON005 g169090 BLASTN 351 1e−46 76 3170 16 700752256H1 SOYMON014 g309670 BLASTN 374 1e−46 80 3171 16 700907488H1 SOYMON022 g169090 BLASTN 467 1e−46 82 3172 16 701146736H1 SOYMON031 g19565 BLASTN 568 1e−46 81 3173 16 700872466H1 SOYMON018 g20732 BLASTN 596 1e−46 81 3174 16 701057780H1 SOYMON033 g169090 BLASTN 610 1e−46 87 3175 16 701145459H1 SOYMON031 g169090 BLASTN 660 1e−46 88 3176 16 701210858H1 SOYMON035 g19565 BLASTN 660 1e−46 84 3177 16 700877001H1 SOYMON018 g20732 BLASTN 662 1e−46 77 3178 16 700742465H1 SOYMON012 g169090 BLASTN 664 1e−46 86 3179 16 700763342H1 SOYMON015 g169090 BLASTN 668 1e−46 79 3180 16 700685380H1 SOYMON008 g20732 BLASTN 669 1e−46 78 3181 16 701149865H1 SOYMON031 g2905771 BLASTN 330 1e−45 100 3182 16 700891972H1 SOYMON024 g169090 BLASTN 434 1e−45 78 3183 16 700750391H1 SOYMON013 g169090 BLASTN 436 1e−45 78 3184 16 700683883H1 SOYMON008 g169090 BLASTN 436 1e−45 84 3185 16 700729088H1 SOYMON009 g2078297 BLASTN 509 1e−45 85 3186 16 700903141H1 SOYMON022 g19565 BLASTN 577 1e−45 84 3187 16 701202337H1 SOYMON035 g169090 BLASTN 603 1e−45 84 3188 16 701155013H1 SOYMON031 g19565 BLASTN 647 1e−45 86 3189 16 700844326H1 SOYMON021 g19565 BLASTN 651 1e−45 86 3190 16 700741362H1 SOYMON012 g169090 BLASTN 651 1e−45 84 3191 16 700755283H1 SOYMON014 g169090 BLASTN 652 1e−45 87 3192 16 700751536H1 SOYMON014 g20732 BLASTN 652 1e−45 79 3193 16 700684196H1 SOYMON008 g20732 BLASTN 654 1e−45 79 3194 16 700684881H1 SOYMON008 g20732 BLASTN 657 1e−45 92 3195 16 700680531H1 SOYMON008 g20732 BLASTN 429 1e−44 79 3196 16 701106044H1 SOYMON036 g20732 BLASTN 592 1e−44 78 3197 16 700979630H2 SOYMON009 g2905771 BLASTN 618 1e−44 97 3198 16 700751095H1 SOYMON014 g169090 BLASTN 634 1e−44 82 3199 16 701153515H1 SOYMON031 g19565 BLASTN 639 1e−44 85 3200 16 700741789H1 SOYMON012 g20732 BLASTN 641 1e−44 82 3201 16 701204330H2 SOYMON035 g19565 BLASTN 643 1e−44 86 3202 16 700967679H1 SOYMON032 g409574 BLASTN 643 1e−44 83 3203 16 700972372H1 SOYMON005 g169090 BLASTN 644 1e−44 74 3204 16 700974446H1 SOYMON005 g19565 BLASTN 644 1e−44 85 3205 16 701146670H1 SOYMON031 g19565 BLASTN 341 1e−43 81 3206 16 701102507H1 SOYMON028 g169090 BLASTN 432 1e−43 86 3207 16 701006744H1 SOYMON019 g169090 BLASTN 453 1e−43 85 3208 16 700835690H1 SOYMON019 g169090 BLASTN 479 1e−43 84 3209 16 700983742H1 SOYMON009 g169090 BLASTN 529 1e−43 87 3210 16 700654457H1 SOYMON004 g169090 BLASTN 601 1e−43 80 3211 16 700555371H1 SOYMON001 g20732 BLASTN 623 1e−43 78 3212 16 700991260H1 SOYMON011 g19565 BLASTN 623 1e−43 86 3213 16 701109867H1 SOYMON036 g20732 BLASTN 623 1e−43 78 3214 16 701151625H1 SOYMON031 g19565 BLASTN 626 1e−43 84 3215 16 700748787H1 SOYMON013 g169090 BLASTN 630 1e−43 78 3216 16 700754611H1 SOYMON014 g19565 BLASTN 631 1e−43 85 3217 16 700852565H1 SOYMON023 g169090 BLASTN 611 1e−42 78 3218 16 700791713H1 SOYMON011 g20732 BLASTN 612 1e−42 72 3219 16 701205047H1 SOYMON035 g19565 BLASTN 613 1e−42 85 3220 16 700972230H1 SOYMON005 g169090 BLASTN 614 1e−42 79 3221 16 701157734H1 SOYMON031 g19565 BLASTN 617 1e−42 86 3222 16 700567308H1 SOYMON002 g169090 BLASTN 621 1e−42 81 3223 16 700741053H1 SOYMON012 g20732 BLASTN 454 1e−41 83 3224 16 701124645H1 SOYMON037 g19565 BLASTN 505 1e−41 81 3225 16 700738430H1 SOYMON012 g169090 BLASTN 598 1e−41 83 3226 16 700980387H1 SOYMON009 g169090 BLASTN 607 1e−41 86 3227 16 701109905H1 SOYMON036 g169090 BLASTN 609 1e−41 87 3228 16 700756857H1 SOYMON014 g169090 BLASTN 352 1e−40 80 3229 16 700685415H1 SOYMON008 g20732 BLASTN 373 1e−40 83 3230 16 700999463H1 SOYMON018 g20732 BLASTN 373 1e−40 79 3231 16 700899494H1 SOYMON027 g169090 BLASTN 472 1e−40 88 3232 16 701152616H1 SOYMON031 g19565 BLASTN 587 1e−40 84 3233 16 700682787H1 SOYMON008 g20732 BLASTN 588 1e−40 75 3234 16 700997526H1 SOYMON018 g20732 BLASTN 588 1e−40 88 3235 16 701152717H1 SOYMON031 g19565 BLASTN 589 1e−40 87 3236 16 701156106H1 SOYMON031 g19565 BLASTN 590 1e−40 87 3237 16 700757283H1 SOYMON015 g169090 BLASTN 592 1e−40 75 3238 16 701153845H1 SOYMON031 g19565 BLASTN 595 1e−40 87 3239 16 701152664H1 SOYMON031 g19565 BLASTN 596 1e−40 86 3240 16 700960557H1 SOYMON022 g169090 BLASTN 280 1e−39 82 3241 16 701046409H1 SOYMON032 g409574 BLASTN 371 1e−39 76 3242 16 700648740H1 SOYMON003 g409574 BLASTN 385 1e−39 89 3243 16 700728066H1 SOYMON009 g169090 BLASTN 461 1e−39 73 3244 16 700740668H1 SOYMON012 g20732 BLASTN 575 1e−39 73 3245 16 701149559H1 SOYMON031 g19565 BLASTN 575 1e−39 86 3246 16 701124058H1 SOYMON037 g20732 BLASTN 576 1e−39 80 3247 16 701154958H1 SOYMON031 g19565 BLASTN 577 1e−39 86 3248 16 701149995H1 SOYMON031 g19565 BLASTN 583 1e−39 87 3249 16 701145383H1 SOYMON031 g19565 BLASTN 585 1e−39 84 3250 16 701064544H1 SOYMON034 g2905771 BLASTN 326 1e−38 93 3251 16 700992479H1 SOYMON011 g2078297 BLASTN 374 1e−38 80 3252 16 700739262H1 SOYMON012 g20732 BLASTN 441 1e−38 80 3253 16 700999632H1 SOYMON018 g20732 BLASTN 509 1e−38 79 3254 16 700743974H1 SOYMON012 g20732 BLASTN 562 1e−38 80 3255 16 700835707H1 SOYMON019 g169090 BLASTN 562 1e−38 86 3256 16 700844641H1 SOYMON021 g19565 BLASTN 562 1e−38 88 3257 16 701048040H1 SOYMON032 g169090 BLASTN 571 1e−38 87 3258 16 700829978H1 SOYMON019 g19565 BLASTN 573 1e−38 84 3259 16 700875006H1 SOYMON018 g20732 BLASTN 336 1e−37 91 3260 16 700830281H1 SOYMON019 g19565 BLASTN 376 1e−37 83 3261 16 700990514H1 SOYMON011 g20732 BLASTN 550 1e−37 79 3262 16 701153744H1 SOYMON031 g19565 BLASTN 557 1e−37 88 3263 16 700742768H1 SOYMON012 g169090 BLASTN 558 1e−37 90 3264 16 701149314H1 SOYMON031 g19565 BLASTN 559 1e−37 88 3265 16 700961862H1 SOYMON022 g169090 BLASTN 559 1e−37 86 3266 16 700875647H1 SOYMON018 g20732 BLASTN 560 1e−37 81 3267 16 700958014H1 SOYMON022 g19565 BLASTN 465 1e−36 81 3268 16 700854826H1 SOYMON023 g2905771 BLASTN 517 1e−36 95 3269 16 701106984H1 SOYMON036 g20732 BLASTN 539 1e−36 79 3270 16 700740352H1 SOYMON012 g20732 BLASTN 539 1e−36 79 3271 16 700903658H1 SOYMON022 g19565 BLASTN 542 1e−36 85 3272 16 700756593H1 SOYMON014 g19565 BLASTN 545 1e−36 88 3273 16 700789341H2 SOYMON011 g169090 BLASTN 546 1e−36 86 3274 16 700751528H1 SOYMON014 g20732 BLASTN 549 1e−36 78 3275 16 701046242H1 SOYMON032 g169090 BLASTN 549 1e−36 86 3276 16 700606131H2 SOYMON008 g20732 BLASTN 257 1e−35 80 3277 16 701063749H1 SOYMON034 g2905771 BLASTN 355 1e−35 97 3278 16 701156830H1 SOYMON031 g19565 BLASTN 401 1e−35 88 3279 16 701123759H1 SOYMON037 g20732 BLASTN 527 1e−35 77 3280 16 700833470H1 SOYMON019 g19565 BLASTN 533 1e−35 86 3281 16 701043561H1 SOYMON029 g169090 BLASTN 307 1e−34 81 3282 16 700685547H1 SOYMON008 g20732 BLASTN 352 1e−34 77 3283 16 701215104H1 SOYMON035 g169090 BLASTN 424 1e−34 87 3284 16 701156675H1 SOYMON031 g169090 BLASTN 439 1e−34 84 3285 16 700650109H1 SOYMON003 g169090 BLASTN 505 1e−34 83 3286 16 700996816H1 SOYMON018 g20732 BLASTN 514 1e−34 89 3287 16 700875986H1 SOYMON018 g20732 BLASTN 517 1e−34 79 3288 16 700875036H1 SOYMON018 g20732 BLASTN 520 1e−34 79 3289 16 700760859H1 SOYMON015 g169090 BLASTN 521 1e−34 85 3290 16 701203868H1 SOYMON035 g19565 BLASTN 522 1e−34 75 3291 16 700684625H1 SOYMON008 g20732 BLASTN 523 1e−34 88 3292 16 700743827H1 SOYMON012 g20550 BLASTN 277 1e−33 84 3293 16 700895366H1 SOYMON027 g20732 BLASTN 509 1e−33 71 3294 16 701155325H1 SOYMON031 g169090 BLASTN 393 1e−32 78 3295 16 700979884H2 SOYMON009 g19565 BLASTN 493 1e−32 87 3296 16 700956948H1 SOYMON022 g19565 BLASTN 497 1e−32 82 3297 16 700983542H1 SOYMON009 g19565 BLASTN 326 1e−31 76 3298 16 700750157H1 SOYMON013 g169090 BLASTN 483 1e−31 79 3299 16 700856401H1 SOYMON023 g19565 BLASTN 485 1e−31 79 3300 16 701153529H1 SOYMON031 g19565 BLASTN 487 1e−31 89 3301 16 700740510H1 SOYMON012 g169090 BLASTN 404 1e−30 84 3302 16 700742952H1 SOYMON012 g20732 BLASTN 472 1e−30 83 3303 16 700754658H1 SOYMON014 g2078297 BLASTN 385 1e−29 85 3304 16 700876748H1 SOYMON018 g20732 BLASTN 457 1e−29 74 3305 16 700673094H1 SOYMON006 g19565 BLASTN 460 1e−29 78 3306 16 700741756H1 SOYMON012 g20732 BLASTN 462 1e−29 79 3307 16 701209936H1 SOYMON035 g169090 BLASTN 464 1e−29 86 3308 16 700997818H1 SOYMON018 g20732 BLASTN 473 1e−29 78 3309 16 701150960H1 SOYMON031 g169090 BLASTN 447 1e−28 83 3310 16 700685752H1 SOYMON008 g20732 BLASTN 467 1e−28 80 3311 16 700981608H1 SOYMON009 g20732 BLASTN 467 1e−28 80 3312 16 700742082H1 SOYMON012 g20732 BLASTN 322 1e−27 83 3313 16 701146456H1 SOYMON031 g169090 BLASTN 352 1e−27 86 3314 16 700977936H1 SOYMON009 g2905771 BLASTN 423 1e−27 98 3315 16 700897772H1 SOYMON027 g20732 BLASTN 446 1e−27 83 3316 16 701064028H1 SOYMON034 g20732 BLASTN 454 1e−27 82 3317 16 701044915H1 SOYMON032 g19565 BLASTN 316 1e−26 88 3318 16 700976839H1 SOYMON009 g2905771 BLASTN 423 1e−26 98 3319 16 700830091H1 SOYMON019 g19565 BLASTN 426 1e−26 86 3320 16 700961412H1 SOYMON022 g19565 BLASTN 427 1e−26 83 3321 16 701104716H1 SOYMON036 g20732 BLASTN 441 1e−26 81 3322 16 700738003H1 SOYMON012 g19565 BLASTN 413 1e−25 87 3323 16 700908925H1 SOYMON022 g21142 BLASTN 262 1e−24 87 3324 16 701130161H1 SOYMON037 g19565 BLASTN 398 1e−24 75 3325 16 700754740H1 SOYMON014 g309670 BLASTN 304 1e−21 76 3326 16 700990677H1 SOYMON011 g169090 BLASTN 361 1e−21 88 3327 16 700662952H1 SOYMON005 g19565 BLASTN 349 1e−20 86 3328 16 700890971H1 SOYMON024 g2905771 BLASTN 355 1e−20 100 3329 16 700745113H1 SOYMON013 g166705 BLASTN 376 1e−20 86 3330 16 700683049H1 SOYMON008 g256965 BLASTX 95 1e−19 72 3331 16 701043808H1 SOYMON032 g2078297 BLASTN 192 1e−17 76 3332 16 700563254H1 SOYMON002 g2905771 BLASTN 326 1e−17 99 3333 16 701068370H1 SOYMON034 g2905771 BLASTN 329 1e−17 95 3334 16 700840885H1 SOYMON020 g21066 BLASTX 83 1e−16 77 3335 16 701146974H1 SOYMON031 g18978 BLASTX 99 1e−16 79 3336 16 700874586H1 SOYMON018 g309671 BLASTX 171 1e−16 89 3337 16 701156431H1 SOYMON031 g309671 BLASTX 172 1e−16 68 3338 16 700731566H1 SOYMON010 g1185556 BLASTX 152 1e−15 91 3339 16 700739659H1 SOYMON012 g309671 BLASTX 161 1e−15 71 3340 16 700678096H1 SOYMON007 g169090 BLASTN 177 1e−15 81 3341 16 700957692H1 SOYMON022 g1185556 BLASTX 147 1e−14 88 3342 16 700554603H1 SOYMON001 g20732 BLASTN 195 1e−14 81 3343 16 701126861H1 SOYMON037 g19565 BLASTN 246 1e−14 85 3344 16 700679091H2 SOYMON007 g166705 BLASTN 266 1e−13 76 3345 16 700737463H1 SOYMON010 g1185556 BLASTX 130 1e−12 89 3346 16 700870957H1 SOYMON018 g309670 BLASTN 282 1e−12 80 3347 16 700651065H1 SOYMON003 g2905772 BLASTX 121 1e−11 100 3348 16 701064564H1 SOYMON034 g1185556 BLASTX 123 1e−11 89 3349 16 701000079H1 SOYMON018 g1185556 BLASTX 126 1e−11 81 3350 16 700606257H1 SOYMON008 g309671 BLASTX 136 1e−11 72 3351 16 700752373H1 SOYMON014 g19565 BLASTN 270 1e−11 92 3352 16 701130139H1 SOYMON037 g2905772 BLASTX 86 1e−10 96 3353 16 700646156H1 SOYMON012 g1185556 BLASTX 110 1e−9 92 3354 16 700743668H1 SOYMON012 g20551 BLASTX 121 1e−9 85 3355 16 700648908H1 SOYMON003 g19565 BLASTN 217 1e−9 90 3356 16 700563235H1 SOYMON002 g169090 BLASTN 220 1e−9 85 3357 1976 700961292H1 SOYMON022 g496493 BLASTN 1040 1e−77 90 3358 1976 700963585H1 SOYMON022 g496493 BLASTN 1027 1e−76 86 3359 1976 700683563H1 SOYMON008 g496493 BLASTN 1007 1e−75 86 3360 1976 700791132H1 SOYMON011 g496493 BLASTN 949 1e−70 86 3361 1976 700890465H1 SOYMON024 g496493 BLASTN 529 1e−68 87 3362 1976 700983190H1 SOYMON009 g496493 BLASTN 904 1e−66 85 3363 1976 700983490H1 SOYMON009 g496493 BLASTN 887 1e−65 81 3364 1976 700992647H1 SOYMON011 g496493 BLASTN 460 1e−56 85 3365 1976 701128429H1 SOYMON037 g496493 BLASTN 718 1e−51 86 3366 1976 700726390H1 SOYMON009 g496493 BLASTN 694 1e−49 81 3367 1976 700764629H1 SOYMON022 g496493 BLASTN 529 1e−35 83 3368 1976 700729434H1 SOYMON009 g496493 BLASTN 382 1e−34 85 3369 1976 700957553H1 SOYMON022 g496493 BLASTN 520 1e−34 91 3370 2207 700726706H1 SOYMON009 g496493 BLASTN 1080 1e−81 88 3371 2207 700553529H1 SOYMON001 g496493 BLASTN 1041 1e−77 87 3372 2207 700739431H1 SOYMON012 g496493 BLASTN 937 1e−69 85 3373 2207 700875340H1 SOYMON018 g496493 BLASTN 875 1e−64 83 3374 2207 700962678H1 SOYMON022 g496493 BLASTN 844 1e−61 83 3375 2207 701214788H1 SOYMON035 g496493 BLASTN 613 1e−42 80 3376 26781 701213755H1 SOYMON035 g1100222 BLASTN 535 1e−55 79 3377 26781 701213579H1 SOYMON035 g1100222 BLASTN 535 1e−45 79 3378 3953 701061621H1 SOYMON033 g172766 BLASTX 104 1e−12 62 3379 4979 700566452H1 SOYMON002 g166705 BLASTN 1068 1e−80 85 3380 4979 701051147H1 SOYMON032 g166705 BLASTN 993 1e−74 83 3381 4979 700851348H1 SOYMON023 g166705 BLASTN 603 1e−73 87 3382 4979 700851470H1 SOYMON023 g166705 BLASTN 978 1e−72 87 3383 4979 701014769H1 SOYMON019 g166705 BLASTN 979 1e−72 84 3384 4979 700667186H1 SOYMON006 g21065 BLASTN 964 1e−71 86 3385 4979 700734161H1 SOYMON010 g21065 BLASTN 956 1e−70 89 3386 4979 700669545H1 SOYMON006 g166705 BLASTN 783 1e−65 84 3387 4979 700895425H1 SOYMON027 g16021 BLASTN 834 1e−65 82 3388 4979 701050651H1 SOYMON032 g409574 BLASTN 892 1e−65 84 3389 4979 701014770H1 SOYMON019 g409574 BLASTN 680 1e−62 83 3390 4979 700786662H1 SOYMON011 g166709 BLASTN 445 1e−60 85 3391 4979 700974162H1 SOYMON005 g167259 BLASTN 824 1e−59 83 3392 4979 700843984H1 SOYMON021 g16021 BLASTN 801 1e−57 84 3393 4979 700893406H1 SOYMON024 g166705 BLASTN 485 1e−56 82 3394 4979 700740022H1 SOYMON012 g167259 BLASTN 654 1e−56 84 3395 4979 701051962H1 SOYMON032 g166709 BLASTN 509 1e−53 87 3396 4979 700899741H1 SOYMON027 g2078297 BLASTN 746 1e−53 84 3397 4979 700890234H1 SOYMON024 g167259 BLASTN 671 1e−47 82 3398 4979 701043720H1 SOYMON032 g166705 BLASTN 571 1e−38 87 3399 4979 700893919H1 SOYMON024 g1345501 BLASTX 179 1e−17 88 3400 535 701064754H1 SOYMON034 g496493 BLASTN 1077 1e−80 88 3401 535 700660246H1 SOYMON004 g496493 BLASTN 1022 1e−76 90 3402 535 700725553H1 SOYMON009 g496493 BLASTN 978 1e−72 86 3403 535 700906586H1 SOYMON022 g496493 BLASTN 745 1e−62 89 3404 535 700555311H1 SOYMON001 g496493 BLASTN 855 1e−62 78 3405 535 700655860H1 SOYMON004 g496493 BLASTN 792 1e−57 86 3406 535 700656931H1 SOYMON004 g496493 BLASTN 669 1e−46 86 3407 535 700684630H1 SOYMON008 g496493 BLASTN 528 1e−35 83 3408 535 700999674H1 SOYMON018 g1842115 BLASTX 183 1e−18 92 3409 667 700763868H1 SOYMON018 g496493 BLASTN 973 1e−74 83 3410 667 700789653H2 SOYMON011 g496493 BLASTN 928 1e−68 85 3411 667 700986940H1 SOYMON009 g496493 BLASTN 929 1e−68 81 3412 667 700982690H1 SOYMON009 g496493 BLASTN 845 1e−64 85 3413 667 700975608H1 SOYMON009 g496493 BLASTN 875 1e−64 82 3414 667 700874732H1 SOYMON018 g496493 BLASTN 679 1e−63 82 3415 667 700956280H1 SOYMON022 g496493 BLASTN 809 1e−61 84 3416 667 700891885H1 SOYMON024 g496493 BLASTN 816 1e−61 83 3417 667 701145577H1 SOYMON031 g496493 BLASTN 764 1e−60 84 3418 667 700975787H1 SOYMON009 g496493 BLASTN 487 1e−59 83 3419 667 700989677H1 SOYMON011 g496493 BLASTN 590 1e−58 84 3420 667 700941396H1 SOYMON024 g496493 BLASTN 781 1e−58 85 3421 667 700985895H1 SOYMON009 g496493 BLASTN 449 1e−57 82 3422 667 700788465H1 SOYMON011 g496493 BLASTN 800 1e−57 80 3423 667 700898809H1 SOYMON027 g496493 BLASTN 743 1e−55 82 3424 667 700659510H1 SOYMON004 g496493 BLASTN 712 1e−53 83 3425 667 700957466H1 SOYMON022 g496493 BLASTN 477 1e−52 82 3426 667 700957672H1 SOYMON022 g496493 BLASTN 730 1e−52 83 3427 667 700752023H1 SOYMON014 g496493 BLASTN 710 1e−50 79 3428 667 700684123H1 SOYMON008 g496493 BLASTN 657 1e−48 82 3429 667 701204216H2 SOYMON035 g496493 BLASTN 632 1e−46 77 3430 667 700684018H1 SOYMON008 g496493 BLASTN 502 1e−44 83 3431 667 700981833H1 SOYMON009 g496493 BLASTN 320 1e−43 81 3432 667 700685767H1 SOYMON008 g496493 BLASTN 566 1e−38 83 3433 667 701119840H1 SOYMON037 g496493 BLASTN 518 1e−37 82 3434 667 700739439H1 SOYMON012 g496493 BLASTN 535 1e−35 86 3435 667 701108638H1 SOYMON036 g496493 BLASTN 420 1e−26 80 3436 667 700681550H1 SOYMON008 g496493 BLASTN 247 1e−20 82 3437 667 700838733H1 SOYMON020 g474408 BLASTX 185 1e−18 80 3438 667 700874784H1 SOYMON018 g474408 BLASTX 174 1e−17 83 3439 667 700796275H1 SOYMON017 g474408 BLASTX 167 1e−16 83 3440 -GM11584 LIB3049-013- LIB3049 g2905771 BLASTN 257 1e−10 83 Q1-E1-F2 3441 -GM12588 LIB3049-035- LIB3049 g20728 BLASTN 448 1e−35 75 Q1-E1-B2 3442 -GM15977 LIB3054-003- LIB3054 g12158 BLASTN 601 1e−41 70 Q1-N1-B6 3443 -GM1666 LIB3028-009- LIB3028 g169090 BLASTN 647 1e−43 74 Q1-B1-C6 3444 -GM17526 LIB3055-013- LIB3055 g20728 BLASTN 249 1e−22 77 Q1-N1-E4 3445 -GM22093 LIB3030-004- LIB3030 g20551 BLASTX 102 1e−35 75 Q1-B1-G2 3446 -GM41500 LIB3051-097- LIB3051 g2905772 BLASTX 106 1e−25 44 Q1-K1-H1 3447 -GM4481 LIB3039-010- LIB3039 g169090 BLASTN 692 1e−48 65 Q1-E1-B9 3448 -GM5704 LIB3039-017- LIB3039 g166705 BLASTN 276 1e−24 75 Q1-E1-F2 3449 1061 LIB3028-008- LIB3028 g20728 BLASTN 743 1e−99 84 Q1-B1-F6 3450 1061 LIB3053-005- LIB3053 g12158 BLASTN 1302 1e−99 82 Q1-N1-D9 3451 1061 LIB3054-004- LIB3054 g20728 BLASTN 743 1e−92 84 Q1-N1-E12 3452 1061 LIB3053-006- LIB3053 g20728 BLASTN 729 1e−89 80 Q1-N1-E5 3453 1061 LIB3053-006- LIB3053 g12158 BLASTN 1096 1e−82 81 Q1-N1-C11 3454 1061 LIB3028-003- LIB3028 g20728 BLASTN 728 1e−80 86 Q1-B1-D12 3455 1061 LIB3040-023- LIB3040 g12158 BLASTN 741 1e−79 83 Q1-E1-D10 3456 1061 LIB3040-036- LIB3040 g20728 BLASTN 735 1e−71 86 Q1-E1-A12 3457 1061 LIB3055-006- LIB3055 g20728 BLASTN 667 1e−56 83 Q1-N1-B3 3458 1061 LIB3055-002- LIB3055 g20728 BLASTN 735 1e−50 86 Q1-B1-A9 3459 1061 LIB3040-053- LIB3040 g20728 BLASTN 579 1e−43 84 Q1-E1-D5 3460 1392 LIB3051-059- LIB3051 g21142 BLASTN 1165 1e−101 82 Q1-K2-D8 3461 1392 LIB3039-009- LIB3039 g19565 BLASTN 923 1e−68 80 Q1-E1-H2 3462 16 LIB3052-014- LIB3052 g20732 BLASTN 1436 1e−110 84 Q1-N1-E5 3463 16 LIB3055-002- LIB3055 g169090 BLASTN 1404 1e−108 82 Q1-B1-A6 3464 16 LIB3028-004- LIB3028 g169090 BLASTN 1399 1e−107 82 Q1-B1-C2 3465 16 LIB3065-011- LIB3065 g169090 BLASTN 1382 1e−106 83 Q1-N1-E4 3466 16 LIB3053-014- LIB3053 g20732 BLASTN 727 1e−104 82 Q1-N1-D3 3467 16 LIB3051-063- LIB3051 g169090 BLASTN 1150 1e−103 78 Q1-K1-F4 3468 16 LIB3040-052- LIB3040 g169090 BLASTN 1247 1e−102 83 Q1-E1-B5 3469 16 LIB3054-006- LIB3054 g169090 BLASTN 1160 1e−100 83 Q1-N1-C1 3470 16 LIB3052-001- LIB3052 g169090 BLASTN 1142 1e−98 82 Q1-B1-C6 3471 16 LIB3055-004- LIB3055 g20732 BLASTN 690 1e−94 83 Q1-N1-F6 3472 16 LIB3051-087- LIB3051 g169090 BLASTN 1190 1e−94 77 Q1-K1-E1 3473 16 LIB3051-018- LIB3051 g169090 BLASTN 772 1e−91 83 Q1-E1-H11 3474 16 LIB3056-012- LIB3056 g169090 BLASTN 1132 1e−89 77 Q1-N1-H7 3475 16 LIB3052-014- LIB3052 g20732 BLASTN 1027 1e−86 79 Q1-N1-E1 3476 16 LIB3039-015- LIB3039 g169090 BLASTN 1138 1e−86 83 Q1-E1-A12 3477 16 LIB3039-003- LIB3039 g169090 BLASTN 719 1e−85 81 Q1-E1-C4 3478 16 LIB3040-015- LIB3040 g169090 BLASTN 1127 1e−85 82 Q1-E1-H5 3479 16 LIB3040-041- LIB3040 g169090 BLASTN 952 1e−84 80 Q1-E1-A4 3480 16 LIB3040-004- LIB3040 g169090 BLASTN 952 1e−84 79 Q1-E1-E11 3481 16 LIB3039-036- LIB3039 g169090 BLASTN 1110 1e−83 79 Q1-E1-D10 3482 16 LIB3039-030- LIB3039 g169090 BLASTN 1093 1e−82 79 Q1-E1-D5 3483 16 LIB3055-008- LIB3055 g169090 BLASTN 634 1e−81 84 Q1-N1-E2 3484 16 LIB3039-003- LIB3039 g169090 BLASTN 890 1e−81 78 Q1-E1-G1 3485 16 LIB3049-020- LIB3049 g169090 BLASTN 957 1e−81 78 Q1-E1-A4 3486 16 LIB3030-012- LIB3030 g169090 BLASTN 691 1e−80 74 Q1-B1-D5 3487 16 LIB3039-007- LIB3039 g169090 BLASTN 1066 1e−80 78 Q1-E1-F8 3488 16 LIB3056-003- LIB3056 g169090 BLASTN 1070 1e−80 78 Q1-N1-H12 3489 16 LIB3049-044- LIB3049 g169090 BLASTN 958 1e−79 78 Q1-E1-H6 3490 16 LIB3051-042- LIB3051 g169090 BLASTN 1047 1e−78 81 Q1-K1-D7 3491 16 LIB3039-005- LIB3039 g169090 BLASTN 957 1e−77 78 Q1-E1-F7 3492 16 LIB3040-028- LIB3040 g169090 BLASTN 974 1e−77 81 Q1-E1-C3 3493 16 LIB3049-014- LIB3049 g169090 BLASTN 737 1e−76 78 Q1-E1-A10 3494 16 LIB3040-012- LIB3040 g169090 BLASTN 800 1e−76 78 Q1-E1-G8 3495 16 LIB3040-061- LIB3040 g169090 BLASTN 957 1e−76 79 Q1-E11-F6 3496 16 LIB3049-044- LIB3049 g169090 BLASTN 976 1e−75 80 Q1-E1-G1 3497 16 LIB3039-040- LIB3039 g169090 BLASTN 994 1e−74 78 Q1-E1-A8 3498 16 LIB3049-054- LIB3049 g169090 BLASTN 766 1e−73 79 Q1-E1-G11 3499 16 LIB3051-062- LIB3051 g166705 BLASTN 869 1e−73 77 Q1-K1-B9 3500 16 LIB3040-039- LIB3040 g169090 BLASTN 970 1e−72 83 Q1-E1-A5 3501 16 LIB3039-031- LIB3039 g19565 BLASTN 970 1e−72 83 Q1-E1-E11 3502 16 LIB3040-043- LIB3040 g169090 BLASTN 970 1e−72 83 Q1-E1-G3 3503 16 LIB3039-031- LIB3039 g19565 BLASTN 971 1e−72 83 Q1-E1-A7 3504 16 LIB3039-047- LIB3039 g169090 BLASTN 713 1e−71 78 Q1-E1-B12 3505 16 LIB3039-033- LIB3039 g409574 BLASTN 965 1e−71 82 Q1-E1-D8 3506 16 LIB3040-010- LIB3040 g19565 BLASTN 969 1e−71 83 Q1-E1-A11 3507 16 LIB3040-015- LIB3040 g169090 BLASTN 726 1e−70 78 Q1-E1-G5 3508 16 LIB3040-008- LIB3040 g169090 BLASTN 842 1e−70 81 Q1-E1-G6 3509 16 LIB3049-045- LIB3049 g19565 BLASTN 955 1e−70 82 Q1-E1-H2 3510 16 LIB3065-008- LIB3065 g169090 BLASTN 416 1e−69 80 Q1-N1-B3 3511 16 LIB3039-028- LIB3039 g169090 BLASTN 713 1e−69 78 Q1-E1-D6 3512 16 LIB3039-045- LIB3039 g169090 BLASTN 940 1e−69 83 Q1-E1-D5 3513 16 LIB3040-058- LIB3040 g20732 BLASTN 396 1e−68 80 Q1-E1-G12 3514 16 LIB3049-034- LIB3049 g169090 BLASTN 633 1e−67 80 Q1-E1-F1 3515 16 LIB3039-050- LIB3039 g169090 BLASTN 730 1e−67 79 Q1-E1-C11 3516 16 LIB3040-042- LIB3040 g19565 BLASTN 762 1e−67 80 Q1-E1-E12 3517 16 LIB3040-030- LIB3040 g169090 BLASTN 847 1e−67 79 Q1-E1-E11 3518 16 LIB3040-054- LIB3040 g169090 BLASTN 909 1e−67 78 Q1-E1-E9 3519 16 LIB3039-046- LIB3039 g19565 BLASTN 917 1e−67 82 Q1-E1-H3 3520 16 LIB3039-020- LIB3039 g19565 BLASTN 908 1e−66 82 Q1-E1-E1 3521 16 LIB3040-036- LIB3040 g19565 BLASTN 693 1e−63 83 Q1-E1-F9 3522 16 LIB3039-054- LIB3039 g169090 BLASTN 633 1e−62 79 Q1-E1-G11 3523 16 LIB3040-053- LIB3040 g169090 BLASTN 508 1e−60 77 Q1-E1-C6 3524 16 LIB3040-006- LIB3040 g409574 BLASTN 855 1e−60 82 Q1-E1-H9 3525 16 LIB3027-011- LIB3027 g2905771 BLASTN 754 1e−56 97 Q1-B1-C6 3526 16 LIB3039-045- LIB3039 g169090 BLASTN 751 1e−52 73 Q1-E1-E3 3527 16 LIB3039-029- LIB3039 g169090 BLASTN 422 1e−50 80 Q1-E1-D8 3528 16 LIB3049-022- LIB3049 g166705 BLASTN 376 1e−46 79 Q1-E1-G9 3529 16 LIB3039-027- LIB3039 g19565 BLASTN 417 1e−45 83 Q1-E1-C2 3530 16 LIB3040-026- LIB3040 g169090 BLASTN 514 1e−43 69 Q1-E1-C12 3531 16 LIB3040-042- LIB3040 g19565 BLASTN 575 1e−42 80 Q1-E1-E1 3532 16 LIB3039-003- LIB3039 g2905771 BLASTN 422 1e−39 87 Q1-E1-A2 3533 16 LIB3039-048- LIB3039 g169090 BLASTN 422 1e−36 77 Q1-E1-D6 3534 16 LIB3040-018- LIB3040 g22238 BLASTX 79 1e−34 78 Q1-E1-G2 3535 16 LIB3050-020- LIB3050 g19565 BLASTN 549 1e−34 87 Q1-K1-A10 3536 16 LIB3051-022- LIB3051 g19565 BLASTN 480 1e−31 85 Q1-K1-D1 3537 16 LIB3039-051- LIB3039 g1345567 BLASTX 110 1e−28 63 Q1-E1-F10 3538 1976 LIB3053-010- LIB3053 g496493 BLASTN 341 1e−57 83 Q1-N1-B4 3539 33625 LIB3054-008- LIB3054 g20732 BLASTN 227 1e−11 85 Q1-N1-D12 3540 535 LIB3053-009- LIB3053 g496493 BLASTN 808 1e−58 86 Q1-N1-D11 MAIZE TRIOSE PHOSPHATE ISOMERASE 3541 -700019675 700019675H1 SATMON001 g546735 BLASTX 134 1e−11 78 3542 -700073894 700073894H1 SATMON007 g609261 BLASTN 257 1e−10 84 3543 -700167260 700167260H1 SATMON013 g609261 BLASTN 644 1e−44 79 3544 -700380595 700380595H1 SATMON021 g609261 BLASTN 1121 1e−84 87 3545 -700449667 700449667H1 SATMON028 g217973 BLASTN 204 1e−18 93 3546 -700449720 700449720H2 SATMON028 g217973 BLASTN 216 1e−18 88 3547 -700570661 700570661H1 SATMON030 g168647 BLASTX 131 1e−11 88 3548 -700616770 700616770H1 SATMON033 g407525 BLASTX 149 1e−13 83 3549 -701170944 701170944H1 SATMONN05 g217921 BLASTX 188 1e−20 53 3550 11337 700337974H1 SATMON020 g256119 BLASTN 535 1e−61 78 3551 11337 700027829H1 SATMON003 g256119 BLASTN 726 1e−51 80 3552 126 700050046H1 SATMON003 g1785947 BLASTN 440 1e−26 92 3553 282 700077320H1 SATMON007 g217973 BLASTN 666 1e−108 97 3554 282 700104541H1 SATMON010 g217973 BLASTN 631 1e−106 97 3555 282 700047476H1 SATMON003 g217973 BLASTN 648 1e−105 97 3556 282 700211559H1 SATMON016 g217973 BLASTN 525 1e−104 97 3557 282 700073553H1 SATMON007 g217973 BLASTN 981 1e−103 98 3558 282 700613011H1 SATMON033 g217973 BLASTN 552 1e−102 98 3559 282 700352119H1 SATMON023 g217973 BLASTN 666 1e−101 97 3560 282 700088148H1 SATMON011 g217973 BLASTN 666 1e−100 98 3561 282 700351626H1 SATMON023 g217973 BLASTN 401 1e−99 98 3562 282 700240096H1 SATMON010 g217973 BLASTN 666 1e−98 97 3563 282 700083660H1 SATMON011 g217973 BLASTN 666 1e−97 99 3564 282 700208721H1 SATMON016 g217973 BLASTN 497 1e−96 98 3565 282 700203144H1 SATMON003 g217973 BLASTN 511 1e−96 96 3566 282 700430425H1 SATMONN01 g217973 BLASTN 666 1e−96 98 3567 282 700206091H1 SATMON003 g217973 BLASTN 497 1e−94 97 3568 282 700077017H1 SATMON007 g217973 BLASTN 614 1e−93 93 3569 282 700618792H1 SATMON034 g217973 BLASTN 546 1e−92 96 3570 282 700572532H1 SATMON030 g407524 BLASTN 1212 1e−92 84 3571 282 700106512H1 SATMON010 g217973 BLASTN 632 1e−91 97 3572 282 700195031H1 SATMON014 g217973 BLASTN 471 1e−90 97 3573 282 700168131H1 SATMON013 g217973 BLASTN 497 1e−89 98 3574 282 700197039H1 SATMON014 g217973 BLASTN 546 1e−89 98 3575 282 700572688H1 SATMON030 g169820 BLASTN 1114 1e−89 85 3576 282 700021313H1 SATMON001 g217973 BLASTN 913 1e−87 97 3577 282 700452417H1 SATMON028 g217973 BLASTN 425 1e−86 95 3578 282 700346119H1 SATMON021 g217973 BLASTN 444 1e−86 96 3579 282 700082359H1 SATMON011 g217973 BLASTN 542 1e−86 93 3580 282 700240042H1 SATMON010 g217973 BLASTN 596 1e−86 97 3581 282 700030064H1 SATMON003 g217973 BLASTN 587 1e−85 94 3582 282 700615185H1 SATMON033 g217973 BLASTN 430 1e−84 98 3583 282 700196125H1 SATMON014 g217973 BLASTN 581 1e−84 100 3584 282 700243429H1 SATMON010 g217973 BLASTN 632 1e−84 97 3585 282 700474112H1 SATMON025 g217973 BLASTN 570 1e−83 98 3586 282 700572282H1 SATMON030 g407524 BLASTN 838 1e−83 82 3587 282 700622238H1 SATMON034 g169820 BLASTN 917 1e−80 86 3588 282 700095609H1 SATMON008 g169820 BLASTN 1067 1e−80 82 3589 282 700218886H1 SATMON011 g217973 BLASTN 551 1e−79 93 3590 282 700018688H1 SATMON001 g217973 BLASTN 1066 1e−79 99 3591 282 700049775H1 SATMON003 g217973 BLASTN 362 1e−78 91 3592 282 700575972H1 SATMON030 g169820 BLASTN 894 1e−78 79 3593 282 700215519H1 SATMON016 g217973 BLASTN 497 1e−76 97 3594 282 700161120H1 SATMON012 g217973 BLASTN 622 1e−76 98 3595 282 700581760H1 SATMON031 g217973 BLASTN 533 1e−75 90 3596 282 700104672H1 SATMON010 g169820 BLASTN 1012 1e−75 83 3597 282 700346053H1 SATMON021 g169820 BLASTN 1012 1e−75 83 3598 282 701166592H1 SATMONN04 g217973 BLASTN 661 1e−74 95 3599 282 700968667H1 SATMONN04 g217973 BLASTN 497 1e−73 92 3600 282 700205627H1 SATMON003 g217973 BLASTN 666 1e−73 99 3601 282 700029005H1 SATMON003 g169820 BLASTN 979 1e−72 85 3602 282 700476479H1 SATMON025 g169820 BLASTN 554 1e−71 84 3603 282 700050148H1 SATMON003 g169820 BLASTN 608 1e−70 83 3604 282 700259846H1 SATMON017 g217973 BLASTN 283 1e−69 94 3605 282 700344093H1 SATMON021 g169820 BLASTN 934 1e−69 83 3606 282 700082327H1 SATMON011 g169820 BLASTN 943 1e−69 85 3607 282 700020156H1 SATMON001 g217973 BLASTN 420 1e−68 99 3608 282 700577714H1 SATMON031 g169820 BLASTN 928 1e−68 85 3609 282 700104904H1 SATMON010 g169820 BLASTN 913 1e−67 84 3610 282 700104685H1 SATMON010 g169820 BLASTN 897 1e−66 84 3611 282 700053463H1 SATMON009 g169820 BLASTN 907 1e−66 85 3612 282 700171639H1 SATMON013 g217973 BLASTN 401 1e−65 98 3613 282 700574233H1 SATMON030 g169820 BLASTN 651 1e−65 83 3614 282 700262653H1 SATMON017 g169820 BLASTN 877 1e−64 84 3615 282 700456738H1 SATMON029 g169820 BLASTN 877 1e−64 84 3616 282 700611806H1 SATMON022 g169820 BLASTN 877 1e−64 83 3617 282 700381177H1 SATMON023 g169820 BLASTN 884 1e−64 84 3618 282 700103347H1 SATMON010 g169820 BLASTN 861 1e−63 84 3619 282 700103605H1 SATMON010 g169820 BLASTN 868 1e−63 84 3620 282 700578536H1 SATMON031 g169820 BLASTN 856 1e−62 84 3621 282 700258606H1 SATMON017 g169820 BLASTN 807 1e−61 83 3622 282 700335703H1 SATMON019 g217973 BLASTN 376 1e−60 90 3623 282 700351044H1 SATMON023 g169820 BLASTN 471 1e−59 83 3624 282 700346364H1 SATMON021 g169820 BLASTN 813 1e−59 85 3625 282 700619037H1 SATMON034 g169820 BLASTN 814 1e−59 84 3626 282 700465160H1 SATMON025 g169820 BLASTN 751 1e−57 84 3627 282 700235687H1 SATMON010 g169820 BLASTN 791 1e−57 82 3628 282 700105645H1 SATMON010 g169820 BLASTN 793 1e−57 83 3629 282 700082237H1 SATMON011 g169820 BLASTN 793 1e−57 84 3630 282 700261906H1 SATMON017 g169820 BLASTN 796 1e−57 83 3631 282 700456154H1 SATMON029 g169820 BLASTN 799 1e−57 84 3632 282 700047696H1 SATMON003 g169820 BLASTN 561 1e−56 83 3633 282 700449905H1 SATMON028 g169820 BLASTN 788 1e−56 84 3634 282 700336106H1 SATMON019 g217973 BLASTN 325 1e−55 92 3635 282 700381867H1 SATMON023 g2529386 BLASTN 422 1e−55 97 3636 282 700051335H1 SATMON003 g169820 BLASTN 608 1e−55 83 3637 282 700050988H1 SATMON003 g169820 BLASTN 768 1e−55 86 3638 282 700029471H1 SATMON003 g169820 BLASTN 772 1e−55 84 3639 282 700106806H1 SATMON010 g169820 BLASTN 773 1e−55 84 3640 282 700071749H1 SATMON007 g217973 BLASTN 362 1e−54 85 3641 282 700207607H1 SATMON016 g217973 BLASTN 362 1e−54 85 3642 282 700573465H2 SATMON030 g169820 BLASTN 753 1e−54 86 3643 282 700220908H1 SATMON011 g169820 BLASTN 758 1e−54 84 3644 282 700467719H1 SATMON025 g169820 BLASTN 761 1e−54 85 3645 282 700456018H1 SATMON029 g169820 BLASTN 764 1e−54 81 3646 282 700453767H1 SATMON029 g217973 BLASTN 296 1e−52 94 3647 282 700026118H1 SATMON003 g217973 BLASTN 341 1e−52 93 3648 282 700026760H1 SATMON003 g217973 BLASTN 421 1e−52 99 3649 282 700029525H1 SATMON003 g169820 BLASTN 738 1e−52 85 3650 282 700457972H1 SATMON029 g169820 BLASTN 723 1e−51 85 3651 282 700455866H1 SATMON029 g169820 BLASTN 726 1e−51 84 3652 282 700165290H1 SATMON013 g169820 BLASTN 726 1e−51 84 3653 282 700351190H1 SATMON023 g169820 BLASTN 672 1e−50 81 3654 282 700154095H1 SATMON007 g169820 BLASTN 696 1e−49 84 3655 282 700450438H1 SATMON028 g217973 BLASTN 430 1e−48 99 3656 282 700044892H1 SATMON004 g169820 BLASTN 683 1e−48 85 3657 282 700185095H1 SATMON014 g169820 BLASTN 673 1e−47 84 3658 282 700575506H1 SATMON030 g169820 BLASTN 680 1e−47 83 3659 282 700161966H1 SATMON012 g217973 BLASTN 335 1e−46 98 3660 282 700343401H1 SATMON021 g169820 BLASTN 426 1e−45 77 3661 282 700152354H1 SATMON007 g169820 BLASTN 653 1e−45 84 3662 282 701164924H1 SATMONN04 g169820 BLASTN 397 1e−44 84 3663 282 700346896H1 SATMON021 g169820 BLASTN 496 1e−42 84 3664 282 700210157H1 SATMON016 g169820 BLASTN 617 1e−42 84 3665 282 700383103H1 SATMON024 g169820 BLASTN 531 1e−41 84 3666 282 701158829H1 SATMONN04 g407524 BLASTN 549 1e−40 80 3667 282 700619883H1 SATMON034 g217973 BLASTN 325 1e−38 99 3668 282 700168219H1 SATMON013 g169820 BLASTN 540 1e−36 83 3669 282 700155210H1 SATMON007 g169820 BLASTN 545 1e−36 83 3670 282 700334861H1 SATMON019 g169820 BLASTN 484 1e−31 82 3671 282 700355663H1 SATMON024 g217973 BLASTN 213 1e−30 88 3672 282 700074764H1 SATMON007 g546734 BLASTN 387 1e−27 84 3673 282 700621934H1 SATMON034 g217973 BLASTN 430 1e−26 100 3674 282 700802084H1 SATMON036 g217973 BLASTN 270 1e−24 98 3675 3039 700620444H1 SATMON034 g1785947 BLASTN 473 1e−56 75 3676 3039 700356205H1 SATMON024 g1785947 BLASTN 332 1e−32 72 3677 3039 700215549H1 SATMON016 g414549 BLASTN 443 1e−26 72 3678 3039 700620318H1 SATMON034 g556171 BLASTX 214 1e−25 79 3679 3039 700028742H1 SATMON003 g556171 BLASTX 156 1e−20 86 3680 3039 700150060H1 SATMON007 g556171 BLASTX 181 1e−17 89 3681 3039 700448477H1 SATMON027 g556171 BLASTX 137 1e−12 85 3682 3039 700336489H1 SATMON019 g556171 BLASTX 126 1e−10 81 3683 3414 700099709H1 SATMON009 g609261 BLASTN 600 1e−49 84 3684 3414 700075837H1 SATMON007 g609261 BLASTN 494 1e−41 84 3685 3414 700045678H1 SATMON004 g609261 BLASTN 340 1e−29 73 3686 3414 700097852H1 SATMON009 g609261 BLASTN 436 1e−27 84 3687 3414 700053342H1 SATMON009 g609261 BLASTN 346 1e−25 73 3688 3414 700041954H1 SATMON004 g609261 BLASTN 340 1e−24 82 3689 3414 700217471H1 SATMON016 g609261 BLASTN 265 1e−21 71 3690 3414 700264437H1 SATMON017 g609261 BLASTN 231 1e−17 69 3691 3414 700218371H1 SATMON016 g609261 BLASTN 156 1e−10 68 3692 5593 700381686H1 SATMON023 g609261 BLASTN 534 1e−44 89 3693 5593 700356082H1 SATMON024 g609261 BLASTN 246 1e−24 90 3694 5593 700622077H1 SATMON034 g609261 BLASTN 292 1e−20 86 3695 5593 700470822H1 SATMON025 g609262 BLASTX 134 1e−11 79 3696 6525 700083139H1 SATMON011 g256119 BLASTN 880 1e−64 76 3697 6525 700205474H1 SATMON003 g169820 BLASTN 849 1e−62 77 3698 6991 700336856H1 SATMON019 g609261 BLASTN 1131 1e−85 85 3699 6991 700042717H1 SATMON004 g609261 BLASTN 1028 1e−76 85 3700 6991 700379491H1 SATMON020 g609261 BLASTN 995 1e−74 81 3701 6991 700156635H1 SATMON012 g609261 BLASTN 877 1e−64 84 3702 6991 700046340H1 SATMON004 g609261 BLASTN 852 1e−62 84 3703 6991 700081869H1 SATMON011 g609261 BLASTN 266 1e−14 80 3704 6991 700426102H1 SATMONN01 g806312 BLASTX 134 1e−13 89 3705 7384 700613626H1 SATMON033 g609261 BLASTN 920 1e−87 85 3706 7384 700101506H1 SATMON009 g609261 BLASTN 1124 1e−84 85 3707 7384 700206445H1 SATMON003 g609261 BLASTN 987 1e−73 79 3708 7384 700220160H1 SATMON011 g609261 BLASTN 878 1e−64 85 3709 -L1431527 LIB143-004- LIB143 g217973 BLASTN 290 1e−13 93 Q1-E1-C5 3710 -L30613868 LIB3061-017- LIB3061 g217973 BLASTN 182 1e−13 70 Q1-K1-C9 3711 -L30623620 LIB3062-034- LIB3062 g609261 BLASTN 599 1e−39 74 Q1-K1-A8 3712 -L361705 LIB36-021- LIB36 g609261 BLASTN 266 1e−14 80 Q1-E1-E7 3713 23992 LIB3062-056- LIB3062 g1200507 BLASTX 285 1e−64 61 Q1-K1-F9 3714 282 LIB3067-047- LIB3067 g217973 BLASTN 1076 1e−164 96 Q1-K1-H2 3715 282 LIB3067-055- LIB3067 g217973 BLASTN 1076 1e−133 93 Q1-K1-G8 3716 282 LIB3067-059- LIB3067 g169820 BLASTN 1401 1e−115 84 Q1-K1-D10 3717 282 LIB3067-027- LIB3067 g407524 BLASTN 995 1e−113 83 Q1-K1-B10 3718 282 LIB189-032- LIB189 g217973 BLASTN 629 1e−111 93 Q1-E1-H2 3719 282 LIB3059-023- LIB3059 g407524 BLASTN 1436 1e−111 83 Q1-K1-A7 3720 282 LIB3069-016- LIB3069 g169820 BLASTN 1301 1e−107 81 Q1-K1-D9 3721 282 LIB143-006- LIB143 g169820 BLASTN 1373 1e−105 84 Q1-E1-A8 3722 282 LIB3068-054- LIB3068 g169820 BLASTN 1327 1e−102 82 Q1-K1-C11 3723 282 LIB3067-034- LIB3067 g407524 BLASTN 1321 1e−101 83 Q1-K1-B7 3724 282 LIB143-031- LIB143 g169820 BLASTN 1311 1e−100 84 Q1-E1-E5 3725 282 LIB3069-055- LIB3069 g169820 BLASTN 1046 1e−97 75 Q1-K1-H12 3726 282 LIB3061-027- LIB3061 g169820 BLASTN 936 1e−96 83 Q1-K1-A8 3727 282 LIB3078-008- LIB3078 g169820 BLASTN 1210 1e−92 82 Q1-K1-E5 3728 282 LIB3066-027- LIB3066 g407524 BLASTN 1196 1e−91 82 Q1-K1-E1 3729 282 LIB3067-032- LIB3067 g169820 BLASTN 1122 1e−84 84 Q1-K1-E5 3730 282 LIB3078-029- LIB3078 g169820 BLASTN 827 1e−83 82 Q1-K1-F7 3731 282 LIB3061-006- LIB3061 g169820 BLASTN 1091 1e−82 78 Q1-K1-B7 3732 282 LIB143-048- LIB143 g169820 BLASTN 644 1e−74 75 Q1-E1-F8 3733 282 LIB3078-033- LIB3078 g169820 BLASTN 584 1e−73 79 Q1-K1-B10 3734 282 LIB3069-046- LIB3069 g169820 BLASTN 819 1e−59 79 Q1-K1-C4 3735 282 LIB3061-049- LIB3061 g169820 BLASTN 587 1e−47 80 Q1-K1-H2 3736 282 LIB143-029- LIB143 g169820 BLASTN 679 1e−47 84 Q1-E1-G4 3737 282 LIB84-027- LIB84 g169820 BLASTN 613 1e−46 78 Q1-E1-E5 3738 282 LIB3062-001- LIB3062 g169820 BLASTN 507 1e−33 80 Q1-K2-F7 3739 282 LIB3066-014- LIB3066 g169820 BLASTN 385 1e−25 76 Q1-K1-H11 3740 29645 LIB3069-014- LIB3069 g168647 BLASTX 131 1e−27 34 Q1-K1-C11 3741 29645 LIB3069-013- LIB3069 g168647 BLASTX 124 1e−24 33 Q1-K1-C11 3742 3039 LIB3062-045- LIB3062 g1785947 BLASTN 1119 1e−84 72 Q1-K1-F6 3743 5593 LIB3067-045- LIB3067 g609261 BLASTN 702 1e−58 75 Q1-K1-E5 3744 6991 LIB3059-026- LIB3059 g609261 BLASTN 1493 1e−115 84 Q1-K1-G9 3745 6991 LIB3078-049- LIB3078 g609261 BLASTN 747 1e−55 83 Q1-K1-E4 3746 7384 LIB3062-034- LIB3062 g609261 BLASTN 1351 1e−107 85 Q1-K1-A4 SOYBEAN TRIOSE PHOSPHATE ISOMERASE 3747 -700743237 700743237H1 SOYMON012 g407525 BLASTX 173 1e−17 91 3748 -700977730 700977730H1 SOYMON009 g602589 BLASTN 373 1e−20 71 3749 -701056176 701056176H1 SOYMON032 g806311 BLASTN 752 1e−53 74 3750 -701110172 701110172H1 SOYMON036 g806311 BLASTN 801 1e−57 78 3751 10244 700995141H1 SOYMON011 g806311 BLASTN 470 1e−30 87 3752 10244 701124548H1 SOYMON037 g806311 BLASTN 490 1e−30 88 3753 10244 700739771H1 SOYMON012 g806311 BLASTN 329 1e−16 77 3754 10244 700999820H1 SOYMON018 g806312 BLASTX 147 1e−13 84 3755 10244 701119858H1 SOYMON037 g806312 BLASTX 118 1e−9 72 3756 10535 700988684H1 SOYMON009 g806311 BLASTN 905 1e−66 79 3757 10535 700902425H1 SOYMON027 g806311 BLASTN 872 1e−63 80 3758 1357 701069004H1 SOYMON034 g806311 BLASTN 832 1e−60 81 3759 1357 701151554H1 SOYMON031 g806311 BLASTN 568 1e−38 82 3760 1357 700659936H1 SOYMON004 g806311 BLASTN 545 1e−36 79 3761 16 700680927H1 SOYMON008 g256119 BLASTN 1020 1e−81 78 3762 16 700656871H1 SOYMON004 g256119 BLASTN 903 1e−66 81 3763 16 701124364H1 SOYMON037 g256119 BLASTN 872 1e−64 80 3764 16 701134707H2 SOYMON038 g256119 BLASTN 874 1e−64 81 3765 16 700673750H1 SOYMON007 g256119 BLASTN 781 1e−60 81 3766 16 701123269H1 SOYMON037 g602589 BLASTN 819 1e−59 78 3767 16 701004846H1 SOYMON019 g256119 BLASTN 801 1e−58 80 3768 16 700993362H1 SOYMON011 g256119 BLASTN 808 1e−58 80 3769 16 701005445H1 SOYMON019 g256119 BLASTN 630 1e−56 78 3770 16 701134327H1 SOYMON038 g602589 BLASTN 782 1e−56 79 3771 16 701148169H1 SOYMON031 g602589 BLASTN 574 1e−51 76 3772 16 701153410H1 SOYMON031 g602589 BLASTN 451 1e−50 80 3773 16 700830168H1 SOYMON019 g256119 BLASTN 705 1e−50 77 3774 16 701120627H1 SOYMON037 g602589 BLASTN 715 1e−50 78 3775 16 700975358H1 SOYMON009 g602589 BLASTN 628 1e−49 77 3776 16 700755979H1 SOYMON014 g602589 BLASTN 697 1e−49 79 3777 16 701131374H1 SOYMON038 g602589 BLASTN 703 1e−49 79 3778 16 700994166H1 SOYMON011 g602589 BLASTN 513 1e−47 77 3779 16 701138038H1 SOYMON038 g602589 BLASTN 672 1e−47 77 3780 16 700974248H1 SOYMON005 g602589 BLASTN 658 1e−46 77 3781 16 700655832H1 SOYMON004 g602589 BLASTN 664 1e−46 78 3782 16 700758320H1 SOYMON015 g602589 BLASTN 409 1e−45 80 3783 16 701064709H1 SOYMON034 g602589 BLASTN 477 1e−45 78 3784 16 701138504H1 SOYMON038 g602589 BLASTN 591 1e−45 76 3785 16 700980284H1 SOYMON009 g602589 BLASTN 652 1e−45 79 3786 16 701133585H2 SOYMON038 g602589 BLASTN 634 1e−44 78 3787 16 700674706H1 SOYMON007 g602589 BLASTN 634 1e−44 78 3788 16 700964927H1 SOYMON022 g602589 BLASTN 639 1e−44 78 3789 16 700830923H1 SOYMON019 g602589 BLASTN 626 1e−43 76 3790 16 700662845H1 SOYMON005 g602589 BLASTN 617 1e−42 76 3791 16 701133824H1 SOYMON038 g602589 BLASTN 619 1e−42 78 3792 16 700848913H1 SOYMON021 g602589 BLASTN 603 1e−41 77 3793 16 701005984H1 SOYMON019 g602589 BLASTN 604 1e−41 78 3794 16 701140769H1 SOYMON038 g602589 BLASTN 605 1e−41 76 3795 16 700753357H1 SOYMON014 g602589 BLASTN 328 1e−40 78 3796 16 701056336H1 SOYMON032 g602589 BLASTN 344 1e−40 77 3797 16 700895411H1 SOYMON027 g602589 BLASTN 593 1e−40 78 3798 16 701060188H1 SOYMON033 g602589 BLASTN 277 1e−39 80 3799 16 700739461H1 SOYMON012 g602589 BLASTN 573 1e−39 77 3800 16 700941104H1 SOYMON024 g602589 BLASTN 579 1e−39 79 3801 16 700732960H1 SOYMON010 g602589 BLASTN 581 1e−39 78 3802 16 700686476H1 SOYMON008 g602589 BLASTN 583 1e−39 79 3803 16 701054231H1 SOYMON032 g602589 BLASTN 583 1e−39 77 3804 16 700671690H1 SOYMON006 g602589 BLASTN 566 1e−38 77 3805 16 700941174H1 SOYMON024 g602589 BLASTN 569 1e−38 78 3806 16 701125091H1 SOYMON037 g256119 BLASTN 358 1e−37 74 3807 16 700989827H1 SOYMON011 g602589 BLASTN 555 1e−37 78 3808 16 700835006H1 SOYMON019 g602589 BLASTN 555 1e−37 75 3809 16 700834847H1 SOYMON019 g602589 BLASTN 559 1e−37 78 3810 16 700953411H1 SOYMON022 g602589 BLASTN 314 1e−36 80 3811 16 700869222H1 SOYMON016 g602589 BLASTN 541 1e−36 78 3812 16 700850633H1 SOYMON023 g602589 BLASTN 544 1e−36 78 3813 16 700890283H1 SOYMON024 g602589 BLASTN 310 1e−35 80 3814 16 700727079H1 SOYMON009 g414549 BLASTN 358 1e−35 73 3815 16 700892544H1 SOYMON024 g602589 BLASTN 486 1e−35 78 3816 16 700869230H1 SOYMON016 g602589 BLASTN 528 1e−35 78 3817 16 700993034H1 SOYMON011 g602589 BLASTN 518 1e−34 75 3818 16 700975553H1 SOYMON009 g414549 BLASTN 524 1e−34 79 3819 16 700651326H1 SOYMON003 g602589 BLASTN 356 1e−33 80 3820 16 701215308H1 SOYMON035 g414549 BLASTN 450 1e−33 75 3821 16 700654480H1 SOYMON004 g414549 BLASTN 511 1e−33 80 3822 16 701045128H1 SOYMON032 g414549 BLASTN 512 1e−33 78 3823 16 701060759H1 SOYMON033 g414549 BLASTN 513 1e−33 80 3824 16 700741652H1 SOYMON012 g602589 BLASTN 493 1e−32 79 3825 16 700675469H1 SOYMON007 g602589 BLASTN 494 1e−32 78 3826 16 700983693H1 SOYMON009 g414549 BLASTN 495 1e−32 80 3827 16 701156784H1 SOYMON031 g602589 BLASTN 495 1e−32 78 3828 16 701009957H2 SOYMON019 g414549 BLASTN 495 1e−32 80 3829 16 700657787H1 SOYMON004 g414549 BLASTN 495 1e−32 79 3830 16 700893935H1 SOYMON024 g602589 BLASTN 481 1e−31 79 3831 16 701144619H1 SOYMON031 g414549 BLASTN 485 1e−31 78 3832 16 701148851H1 SOYMON031 g602589 BLASTN 487 1e−31 79 3833 16 701058218H1 SOYMON033 g602589 BLASTN 495 1e−31 78 3834 16 700975165H1 SOYMON009 g414549 BLASTN 466 1e−30 80 3835 16 701100165H1 SOYMON028 g602589 BLASTN 485 1e−30 79 3836 16 701150241H1 SOYMON031 g602589 BLASTN 455 1e−29 79 3837 16 701098308H1 SOYMON028 g414549 BLASTN 460 1e−29 79 3838 16 701150440H1 SOYMON031 g602589 BLASTN 462 1e−29 78 3839 16 700685125H1 SOYMON008 g414549 BLASTN 471 1e−29 81 3840 16 701061565H1 SOYMON033 g414549 BLASTN 471 1e−29 81 3841 16 700991418H1 SOYMON011 g602589 BLASTN 394 1e−28 68 3842 16 701156156H1 SOYMON031 g602589 BLASTN 456 1e−28 78 3843 16 701007231H2 SOYMON019 g602589 BLASTN 461 1e−28 79 3844 16 700829667H1 SOYMON019 g414549 BLASTN 333 1e−27 73 3845 16 701156033H1 SOYMON031 g602589 BLASTN 432 1e−27 78 3846 16 701014293H1 SOYMON019 g414549 BLASTN 446 1e−27 77 3847 16 700945665H1 SOYMON024 g414549 BLASTN 450 1e−27 81 3848 16 701152138H1 SOYMON031 g414549 BLASTN 450 1e−27 81 3849 16 701001407H1 SOYMON018 g169820 BLASTN 219 1e−26 72 3850 16 700983185H1 SOYMON009 g414549 BLASTN 435 1e−26 72 3851 16 700752364H1 SOYMON014 g414549 BLASTN 441 1e−26 76 3852 16 700992409H1 SOYMON011 g414549 BLASTN 427 1e−25 75 3853 16 701109396H1 SOYMON036 g414549 BLASTN 420 1e−24 76 3854 16 701151402H1 SOYMON031 g556171 BLASTX 151 1e−23 85 3855 16 701149617H1 SOYMON031 g556171 BLASTX 158 1e−23 86 3856 16 700747310H1 SOYMON013 g414549 BLASTN 406 1e−23 73 3857 16 701139569H1 SOYMON038 g556171 BLASTX 191 1e−22 84 3858 16 701213275H1 SOYMON035 g602589 BLASTN 255 1e−22 80 3859 16 701157185H1 SOYMON031 g556171 BLASTX 197 1e−20 90 3860 16 700655520H1 SOYMON004 g556171 BLASTX 166 1e−19 86 3861 16 701010779H1 SOYMON019 g556171 BLASTX 173 1e−19 64 3862 16 701044104H1 SOYMON032 g556171 BLASTX 188 1e−19 89 3863 16 700867605H1 SOYMON016 g556171 BLASTX 160 1e−17 70 3864 16 701125521H1 SOYMON037 g414550 BLASTX 166 1e−16 81 3865 16 701058593H1 SOYMON033 g168647 BLASTX 169 1e−16 94 3866 16 701070286H1 SOYMON034 g168647 BLASTX 164 1e−15 91 3867 16 700649007H1 SOYMON003 g414550 BLASTX 152 1e−14 88 3868 16 700876790H1 SOYMON018 g168647 BLASTX 154 1e−14 93 3869 16 700877219H1 SOYMON018 g168647 BLASTX 154 1e−14 93 3870 16 700877212H1 SOYMON018 g168647 BLASTX 154 1e−14 93 3871 16 700760847H1 SOYMON015 g556171 BLASTX 138 1e−13 86 3872 16 700893711H1 SOYMON024 g168647 BLASTX 140 1e−13 82 3873 16 700557532H1 SOYMON001 g256120 BLASTX 115 1e−12 88 3874 16 700793802H1 SOYMON017 g556171 BLASTX 138 1e−12 93 3875 16 700659725H1 SOYMON004 g556171 BLASTX 144 1e−12 47 3876 16 701044545H1 SOYMON032 g556171 BLASTX 144 1e−12 92 3877 16 701037485H1 SOYMON029 g556171 BLASTX 135 1e−11 96 3878 16 700683524H1 SOYMON008 g168647 BLASTX 136 1e−11 90 3879 16 700876711H1 SOYMON018 g168647 BLASTX 109 1e−10 85 3880 16 701155437H1 SOYMON031 g556171 BLASTX 130 1e−10 92 3881 28599 700997892H1 SOYMON018 g806311 BLASTN 834 1e−60 78 3882 31 701053174H1 SOYMON032 g806311 BLASTN 572 1e−37 73 3883 31 700754467H1 SOYMON014 g806312 BLASTX 145 1e−21 66 3884 31 701107430H1 SOYMON036 g806312 BLASTX 199 1e−20 63 3885 31 700985855H1 SOYMON009 g806312 BLASTX 145 1e−18 64 3886 31 701038167H1 SOYMON029 g806312 BLASTX 179 1e−17 61 3887 31 700670393H1 SOYMON006 g806312 BLASTX 167 1e−16 78 3888 31 700559280H1 SOYMON001 g609262 BLASTX 164 1e−15 69 3889 31 700793048H1 SOYMON017 g806312 BLASTX 97 1e−12 60 3890 31 700993683H1 SOYMON011 g806312 BLASTX 103 1e−11 60 3891 31 700663233H1 SOYMON005 g806312 BLASTX 130 1e−11 56 3892 31 700908079H1 SOYMON022 g806312 BLASTX 103 1e−10 60 3893 31 701043447H1 SOYMON029 g609262 BLASTX 126 1e−10 84 3894 31 700740188H1 SOYMON012 g806312 BLASTX 103 1e−8 60 3895 7466 700742922H1 SOYMON012 g806311 BLASTN 435 1e−27 76 3896 7466 700606255H1 SOYMON008 g806312 BLASTX 117 1e−17 80 3897 16 LIB3053-005- LIB3053 g602589 BLASTN 1000 1e−74 77 Q1-N1-F9 3898 16 LIB3039-035- LIB3039 g602589 BLASTN 979 1e−72 78 Q1-E1-C5 3899 16 LIB3039-031- LIB3039 g256119 BLASTN 911 1e−71 80 Q1-E1-A8 3900 16 LIB3030-003- LIB3030 g602589 BLASTN 949 1e−70 78 Q1-B1-C9 3901 16 LIB3039-023- LIB3039 g602589 BLASTN 913 1e−67 78 Q1-E1-H12 3902 16 LIB3039-047- LIB3039 g602589 BLASTN 566 1e−65 75 Q1-E1-D8 3903 16 LIB3039-052- LIB3039 g602589 BLASTN 890 1e−65 77 Q1-E1-D6 3904 16 LIB3039-051- LIB3039 g602589 BLASTN 855 1e−62 78 Q1-E1-A1 3905 16 LIB3049-009- LIB3049 g602589 BLASTN 783 1e−56 78 Q1-E1-G5 3906 16 LIB3039-009- LIB3039 g602589 BLASTN 805 1e−56 78 Q1-E1-C1 3907 16 LIB3055-006- LIB3055 g256119 BLASTN 481 1e−54 78 Q1-N1-H3 3908 16 LIB3055-013- LIB3055 g256119 BLASTN 769 1e−54 79 Q1-N1-C3 3909 16 LIB3049-034- LIB3049 g602589 BLASTN 626 1e−51 76 Q1-E1-A2 3910 16 LIB3049-022- LIB3049 g602589 BLASTN 519 1e−43 78 Q1-E1-F9 3911 16 LIB3049-030- LIB3049 g602589 BLASTN 572 1e−38 77 Q1-E1-C7 3912 16 LIB3040-035- LIB3040 g556171 BLASTX 175 1e−33 82 Q1-E1-C5 3913 16 LIB3040-005- LIB3040 g169820 BLASTN 324 1e−33 76 Q1-E1-H8 3914 16 LIB3028-025- LIB3028 g602589 BLASTN 464 1e−33 78 Q1-B1-D1 3915 16 LIB3039-022- LIB3039 g602589 BLASTN 357 1e−32 73 Q1-E1-D5 3916 16 LIB3052-001- LIB3052 g414549 BLASTN 327 1e−29 73 Q1-B1-C5 3917 28599 LIB3039-047- LIB3039 g806311 BLASTN 1183 1e−94 81 Q1-E1-D9 3918 28599 LIB3039-048- LIB3039 g806311 BLASTN 1007 1e−92 81 Q1-E1-D12 MAIZE ALDOLASE 3919 -700026544 700026544H1 SATMON003 g22144 BLASTN 215 1e−30 88 3920 -700073329 700073329H1 SATMON007 g22144 BLASTN 590 1e−89 95 3921 -700151987 700151987H1 SATMON007 g22144 BLASTN 212 1e−8 78 3922 -700206575 700206575H1 SATMON003 g22144 BLASTN 1009 1e−109 96 3923 -700333727 700333727H1 SATMON019 g1217893 BLASTX 154 1e−16 61 3924 -700335938 700335938H1 SATMON019 g1730326 BLASTX 76 1e−19 59 3925 -700429795 700429795H1 SATMONN01 g1619605 BLASTX 102 1e−16 77 3926 -700453040 700453040H1 SATMON028 g2213867 BLASTX 96 1e−14 65 3927 -700804137 700804137H1 SATMON036 g22144 BLASTN 742 1e−52 92 3928 1182 700449930H1 SATMON028 g22632 BLASTN 856 1e−62 79 3929 1182 701185559H1 SATMONN06 g22632 BLASTN 793 1e−57 79 3930 1182 700203130H1 SATMON003 g22632 BLASTN 799 1e−57 78 3931 1182 700083459H1 SATMON011 g22632 BLASTN 800 1e−57 76 3932 1182 700465449H1 SATMON025 g22632 BLASTN 405 1e−50 76 3933 1182 701165344H1 SATMONN04 g22632 BLASTN 326 1e−29 78 3934 1461 700101296H1 SATMON009 g218155 BLASTX 164 1e−15 80 3935 1461 700101839H1 SATMON009 g218155 BLASTX 140 1e−12 93 3936 1461 700044840H1 SATMON004 g218155 BLASTX 140 1e−12 93 3937 1461 700045985H1 SATMON004 g218155 BLASTX 140 1e−12 93 3938 1461 700101549H1 SATMON009 g218155 BLASTX 93 1e−11 91 3939 1461 700100334H1 SATMON009 g218155 BLASTX 123 1e−9 59 3940 1461 700100704H1 SATMON009 g218155 BLASTX 112 1e−8 96 3941 28693 700041744H1 SATMON004 g20203 BLASTN 696 1e−49 75 3942 38 700224356H1 SATMON011 g22144 BLASTN 1290 1e−98 96 3943 38 700048169H1 SATMON003 g22144 BLASTN 528 1e−72 98 3944 38 700616610H1 SATMON033 g22144 BLASTN 278 1e−31 91 3945 38 700355765H1 SATMON024 g20204 BLASTX 141 1e−12 96 3946 4416 700342330H1 SATMON021 g218155 BLASTX 96 1e−14 66 3947 4416 700223989H1 SATMON011 g218155 BLASTX 98 1e−10 63 3948 6547 700194431H1 SATMON014 g2636513 BLASTX 181 1e−17 47 3949 6547 700469777H1 SATMON025 g2636513 BLASTX 174 1e−16 48 3950 8494 700426129H1 SATMONN01 g20203 BLASTN 250 1e−20 73 3951 8494 700425929H1 SATMONN01 g927507 BLASTX 67 1e−11 89 3952 -L30603643 LIB3060-046- LIB3060 g169037 BLASTX 155 1e−44 66 Q1-K1-G7 3953 -L30604872 LIB3060-022- LIB3060 g218155 BLASTX 86 1e−27 57 Q1-K1-C10 3954 -L30605671 LIB3060-046- LIB3060 g3695 BLASTN 440 1e−29 71 Q1-K1-B12 3955 1182 LIB3079-006- LIB3079 g22632 BLASTN 598 1e−39 65 Q1-K1-H8 3956 1461 LIB3060-017- LIB3060 g218155 BLASTX 196 1e−41 67 Q1-K1-F3 3957 1461 LIB3059-040- LIB3059 g218155 BLASTX 112 1e−40 84 Q1-K1-C12 3958 1461 LIB3060-030- LIB3060 g218155 BLASTX 112 1e−38 66 Q1-K1-H11 3959 28633 LIB3062-015- LIB3062 g1208898 BLASTX 116 1e−24 45 Q1-K1-G12 3960 28693 LIB3060-018- LIB3060 g20203 BLASTN 926 1e−74 74 Q1-K1-E6 3961 28693 LIB3060-044- LIB3060 g20203 BLASTN 748 1e−62 74 Q1-K1-F10 3962 38 LIB3061-025- LIB3061 g22144 BLASTN 895 1e−133 94 Q1-K1-C9 3963 38 LIB3059-020- LIB3059 g22144 BLASTN 745 1e−53 98 Q1-K1-H3 SOYBEAN ALDOLASE 3964 -700565253 700565253H1 SOYMON002 g3021337 BLASTN 352 1e−39 76 3965 -700865276 700865276H1 SOYMON016 g3021337 BLASTN 629 1e−43 76 3966 -700873022 700873022H1 SOYMON018 g3696 BLASTX 211 1e−26 70 3967 -700943855 700943855H1 SOYMON024 g20204 BLASTX 202 1e−20 86 3968 -700974965 700974965H1 SOYMON005 g3021337 BLASTN 259 1e−10 84 3969 -701039850 701039850H1 SOYMON029 g22632 BLASTN 408 1e−23 76 3970 -701206840 701206840H1 SOYMON035 g3021338 BLASTX 151 1e−13 83 3971 11792 700654881H1 SOYMON004 g20204 BLASTX 150 1e−13 76 3972 11792 700746016H1 SOYMON013 g3021337 BLASTN 284 1e−12 67 3973 12314 701037190H1 SOYMON029 g3021337 BLASTN 634 1e−44 78 3974 12314 701042664H1 SOYMON029 g3021338 BLASTX 197 1e−20 66 3975 16 700651596H1 SOYMON003 g3021337 BLASTN 1101 1e−83 86 3976 16 700750439H1 SOYMON013 g3021337 BLASTN 1078 1e−81 86 3977 16 700649475H1 SOYMON003 g3021337 BLASTN 1082 1e−81 84 3978 16 700652995H1 SOYMON003 g3021337 BLASTN 1084 1e−81 82 3979 16 700981967H1 SOYMON009 g3021337 BLASTN 1071 1e−80 85 3980 16 700863243H1 SOYMON023 g3021337 BLASTN 1044 1e−78 86 3981 16 700558625H1 SOYMON001 g3021337 BLASTN 1041 1e−77 84 3982 16 700564806H1 SOYMON002 g3021337 BLASTN 1021 1e−76 80 3983 16 700746368H1 SOYMON013 g3021337 BLASTN 897 1e−75 86 3984 16 700960290H1 SOYMON022 g3021337 BLASTN 1009 1e−75 87 3985 16 701055132H1 SOYMON032 g3021337 BLASTN 1011 1e−75 86 3986 16 701056109H1 SOYMON032 g3021337 BLASTN 1012 1e−75 84 3987 16 701119884H1 SOYMON037 g3021337 BLASTN 1014 1e−75 87 3988 16 700898149H1 SOYMON027 g3021337 BLASTN 1015 1e−75 86 3989 16 700661436H1 SOYMON005 g3021337 BLASTN 596 1e−74 83 3990 16 701042223H1 SOYMON029 g3021337 BLASTN 997 1e−74 84 3991 16 700676004H1 SOYMON007 g3021337 BLASTN 984 1e−73 85 3992 16 700747718H1 SOYMON013 g3021337 BLASTN 988 1e−73 87 3993 16 700751133H1 SOYMON014 g3021337 BLASTN 989 1e−73 86 3994 16 701215247H1 SOYMON035 g3021337 BLASTN 989 1e−73 84 3995 16 700652484H1 SOYMON003 g3021337 BLASTN 910 1e−72 85 3996 16 700981960H1 SOYMON009 g3021337 BLASTN 970 1e−72 87 3997 16 700869785H1 SOYMON016 g3021337 BLASTN 970 1e−72 87 3998 16 700969335H1 SOYMON005 g3021337 BLASTN 972 1e−72 82 3999 16 700854174H1 SOYMON023 g3021337 BLASTN 965 1e−71 84 4000 16 700761638H1 SOYMON015 g3021337 BLASTN 966 1e−71 86 4001 16 701005716H1 SOYMON019 g3021337 BLASTN 967 1e−71 83 4002 16 700984860H1 SOYMON009 g3021337 BLASTN 967 1e−71 84 4003 16 700941053H1 SOYMON024 g3021337 BLASTN 968 1e−71 86 4004 16 700561358H1 SOYMON002 g3021337 BLASTN 968 1e−71 82 4005 16 700564906H1 SOYMON002 g3021337 BLASTN 562 1e−70 82 4006 16 700833951H1 SOYMON019 g3021337 BLASTN 954 1e−70 88 4007 16 701117626H1 SOYMON037 g3021337 BLASTN 957 1e−70 85 4008 16 700729103H1 SOYMON009 g3021337 BLASTN 535 1e−69 86 4009 16 700670615H1 SOYMON006 g3021337 BLASTN 936 1e−69 83 4010 16 701053635H1 SOYMON032 g3021337 BLASTN 941 1e−69 84 4011 16 700982280H1 SOYMON009 g3021337 BLASTN 923 1e−68 82 4012 16 701119874H1 SOYMON037 g3021337 BLASTN 925 1e−68 88 4013 16 700758937H1 SOYMON015 g3021337 BLASTN 926 1e−68 87 4014 16 701214027H1 SOYMON035 g3021337 BLASTN 928 1e−68 82 4015 16 700972858H1 SOYMON005 g3021337 BLASTN 929 1e−68 84 4016 16 701099780H1 SOYMON028 g3021337 BLASTN 930 1e−68 85 4017 16 700829560H1 SOYMON019 g3021337 BLASTN 932 1e−68 85 4018 16 700971973H1 SOYMON005 g3021337 BLASTN 576 1e−67 85 4019 16 701142336H1 SOYMON038 g3021337 BLASTN 750 1e−67 81 4020 16 701132605H1 SOYMON038 g3021337 BLASTN 759 1e−67 85 4021 16 700969222H1 SOYMON005 g3021337 BLASTN 913 1e−67 84 4022 16 700670956H1 SOYMON006 g3021337 BLASTN 920 1e−67 84 4023 16 701013771H1 SOYMON019 g3021337 BLASTN 921 1e−67 81 4024 16 700895725H1 SOYMON027 g3021337 BLASTN 921 1e−67 84 4025 16 701055481H1 SOYMON032 g3021337 BLASTN 654 1e−66 80 4026 16 700753940H1 SOYMON014 g3021337 BLASTN 899 1e−66 84 4027 16 700974141H1 SOYMON005 g3021337 BLASTN 900 1e−66 81 4028 16 700562408H1 SOYMON002 g3021337 BLASTN 902 1e−66 82 4029 16 700685292H1 SOYMON008 g3021337 BLASTN 903 1e−66 83 4030 16 700985157H1 SOYMON009 g3021337 BLASTN 907 1e−66 82 4031 16 701038194H1 SOYMON029 g3021337 BLASTN 907 1e−66 82 4032 16 700986633H1 SOYMON009 g3021337 BLASTN 908 1e−66 83 4033 16 700564282H1 SOYMON002 g3021337 BLASTN 517 1e−65 83 4034 16 700733754H1 SOYMON010 g3021337 BLASTN 680 1e−65 84 4035 16 700988179H1 SOYMON009 g3021337 BLASTN 887 1e−65 82 4036 16 700555591H1 SOYMON001 g3021337 BLASTN 887 1e−65 82 4037 16 701206717H1 SOYMON035 g3021337 BLASTN 888 1e−65 81 4038 16 700968494H1 SOYMON036 g3021337 BLASTN 889 1e−65 86 4039 16 700677674H1 SOYMON007 g3021337 BLASTN 894 1e−65 83 4040 16 700906271H1 SOYMON022 g3021337 BLASTN 894 1e−65 82 4041 16 700970391H1 SOYMON005 g3021337 BLASTN 896 1e−65 83 4042 16 700753641H1 SOYMON014 g3021337 BLASTN 897 1e−65 82 4043 16 700646593H1 SOYMON014 g3021337 BLASTN 468 1e−64 80 4044 16 700565615H1 SOYMON002 g3021337 BLASTN 667 1e−64 80 4045 16 700746523H1 SOYMON013 g3021337 BLASTN 744 1e−64 83 4046 16 700899019H1 SOYMON027 g3021337 BLASTN 875 1e−64 83 4047 16 701127167H1 SOYMON037 g3021337 BLASTN 876 1e−64 84 4048 16 701131053H1 SOYMON038 g3021337 BLASTN 879 1e−64 84 4049 16 701055811H1 SOYMON032 g3021337 BLASTN 881 1e−64 85 4050 16 700670980H1 SOYMON006 g3021337 BLASTN 881 1e−64 83 4051 16 700900103H1 SOYMON027 g3021337 BLASTN 882 1e−64 83 4052 16 700975609H1 SOYMON009 g3021337 BLASTN 882 1e−64 84 4053 16 701102865H1 SOYMON028 g3021337 BLASTN 883 1e−64 85 4054 16 701145255H1 SOYMON031 g3021337 BLASTN 509 1e−63 80 4055 16 701210875H1 SOYMON035 g3021337 BLASTN 616 1e−63 84 4056 16 700646664H1 SOYMON014 g3021337 BLASTN 862 1e−63 85 4057 16 700897337H1 SOYMON027 g3021337 BLASTN 865 1e−63 86 4058 16 700736783H1 SOYMON010 g3021337 BLASTN 867 1e−63 83 4059 16 701059586H1 SOYMON033 g3021337 BLASTN 869 1e−63 81 4060 16 701127063H1 SOYMON037 g3021337 BLASTN 412 1e−62 84 4061 16 700556614H1 SOYMON001 g3021337 BLASTN 475 1e−62 86 4062 16 700672681H1 SOYMON006 g3021337 BLASTN 818 1e−62 82 4063 16 700727057H1 SOYMON009 g3021337 BLASTN 850 1e−62 82 4064 16 701042141H1 SOYMON029 g3021337 BLASTN 851 1e−62 83 4065 16 700561860H1 SOYMON002 g3021337 BLASTN 854 1e−62 81 4066 16 700677460H1 SOYMON007 g3021337 BLASTN 855 1e−62 83 4067 16 700749578H1 SOYMON013 g3021337 BLASTN 856 1e−62 81 4068 16 700971671H1 SOYMON005 g3021337 BLASTN 856 1e−62 81 4069 16 700672288H1 SOYMON006 g3021337 BLASTN 860 1e−62 81 4070 16 701068481H1 SOYMON034 g3021337 BLASTN 861 1e−62 81 4071 16 700729913H1 SOYMON009 g3021337 BLASTN 661 1e−61 79 4072 16 700739449H1 SOYMON012 g3021337 BLASTN 724 1e−61 85 4073 16 700830902H1 SOYMON019 g3021337 BLASTN 814 1e−61 83 4074 16 700895304H1 SOYMON027 g3021337 BLASTN 840 1e−61 82 4075 16 700605676H2 SOYMON005 g3021337 BLASTN 842 1e−61 84 4076 16 700677453H1 SOYMON007 g3021337 BLASTN 843 1e−61 83 4077 16 700983108H1 SOYMON009 g3021337 BLASTN 843 1e−61 81 4078 16 700889170H1 SOYMON024 g3021337 BLASTN 845 1e−61 86 4079 16 701004956H1 SOYMON019 g3021337 BLASTN 849 1e−61 82 4080 16 700958213H1 SOYMON022 g3021337 BLASTN 849 1e−61 82 4081 16 701129305H1 SOYMON037 g3021337 BLASTN 659 1e−60 85 4082 16 701014446H1 SOYMON019 g3021337 BLASTN 669 1e−60 85 4083 16 700832047H1 SOYMON019 g3021337 BLASTN 738 1e−60 83 4084 16 700669966H1 SOYMON006 g3021337 BLASTN 829 1e−60 82 4085 16 700659491H1 SOYMON004 g3021337 BLASTN 829 1e−60 83 4086 16 701003560H1 SOYMON019 g3021337 BLASTN 829 1e−60 82 4087 16 700758028H1 SOYMON015 g3021337 BLASTN 829 1e−60 81 4088 16 701060964H1 SOYMON033 g3021337 BLASTN 833 1e−60 81 4089 16 700548284H1 SOYMON002 g3021337 BLASTN 834 1e−60 82 4090 16 700894957H1 SOYMON024 g3021337 BLASTN 837 1e−60 81 4091 16 700646551H1 SOYMON014 g3021337 BLASTN 479 1e−59 83 4092 16 700967633H1 SOYMON032 g3021337 BLASTN 530 1e−59 81 4093 16 700754430H1 SOYMON014 g3021337 BLASTN 654 1e−59 85 4094 16 700865919H1 SOYMON016 g3021337 BLASTN 814 1e−59 81 4095 16 700980426H1 SOYMON009 g3021337 BLASTN 815 1e−59 80 4096 16 701048203H1 SOYMON032 g3021337 BLASTN 816 1e−59 81 4097 16 700846414H1 SOYMON021 g3021337 BLASTN 819 1e−59 81 4098 16 700851608H1 SOYMON023 g3021337 BLASTN 822 1e−59 81 4099 16 700970160H1 SOYMON005 g3021337 BLASTN 822 1e−59 82 4100 16 701206312H1 SOYMON035 g3021337 BLASTN 823 1e−59 85 4101 16 700834462H1 SOYMON019 g3021337 BLASTN 823 1e−59 81 4102 16 700562478H1 SOYMON002 g3021337 BLASTN 487 1e−58 84 4103 16 700788114H1 SOYMON011 g3021337 BLASTN 751 1e−58 83 4104 16 700753792H1 SOYMON014 g3021337 BLASTN 804 1e−58 84 4105 16 700837427H1 SOYMON020 g3021337 BLASTN 805 1e−58 86 4106 16 700753668H1 SOYMON014 g3021337 BLASTN 806 1e−58 85 4107 16 700667315H1 SOYMON006 g3021337 BLASTN 809 1e−58 81 4108 16 700808315H1 SOYMON024 g3021337 BLASTN 558 1e−57 80 4109 16 700839033H1 SOYMON020 g3021337 BLASTN 791 1e−57 81 4110 16 700670207H1 SOYMON006 g3021337 BLASTN 791 1e−57 87 4111 16 700849886H1 SOYMON021 g3021337 BLASTN 791 1e−57 83 4112 16 700751117H1 SOYMON014 g3021337 BLASTN 799 1e−57 86 4113 16 700851803H1 SOYMON023 g3021337 BLASTN 799 1e−57 86 4114 16 700669164H1 SOYMON006 g3021337 BLASTN 800 1e−57 80 4115 16 700548285H1 SOYMON002 g3021337 BLASTN 801 1e−57 85 4116 16 701065620H1 SOYMON034 g3021337 BLASTN 426 1e−56 82 4117 16 700727996H1 SOYMON009 g3021337 BLASTN 468 1e−56 79 4118 16 700869176H1 SOYMON016 g3021337 BLASTN 786 1e−56 85 4119 16 700973141H1 SOYMON005 g3021337 BLASTN 440 1e−55 79 4120 16 700969555H1 SOYMON005 g3021337 BLASTN 448 1e−55 81 4121 16 700866138H1 SOYMON016 g3021337 BLASTN 641 1e−55 86 4122 16 700904813H1 SOYMON022 g3021337 BLASTN 699 1e−55 85 4123 16 700669945H1 SOYMON006 g3021337 BLASTN 773 1e−55 86 4124 16 700894146H1 SOYMON024 g3021337 BLASTN 773 1e−55 86 4125 16 701060489H1 SOYMON033 g3021337 BLASTN 664 1e−54 85 4126 16 701125675H1 SOYMON037 g3021337 BLASTN 721 1e−54 85 4127 16 700754750H1 SOYMON014 g3021337 BLASTN 722 1e−54 86 4128 16 701142770H1 SOYMON038 g3021337 BLASTN 755 1e−54 88 4129 16 700731095H1 SOYMON009 g3021337 BLASTN 755 1e−54 87 4130 16 700667966H1 SOYMON006 g3021337 BLASTN 756 1e−54 84 4131 16 700673606H1 SOYMON007 g3021337 BLASTN 760 1e−54 83 4132 16 700965253H1 SOYMON022 g3021337 BLASTN 763 1e−54 86 4133 16 700605289H2 SOYMON003 g3021337 BLASTN 763 1e−54 84 4134 16 700732985H1 SOYMON010 g3021337 BLASTN 765 1e−54 87 4135 16 700986523H1 SOYMON009 g3021337 BLASTN 474 1e−53 85 4136 16 701100040H2 SOYMON028 g3021337 BLASTN 602 1e−53 85 4137 16 700895328H1 SOYMON027 g3021337 BLASTN 742 1e−53 83 4138 16 701141083H1 SOYMON038 g3021337 BLASTN 751 1e−53 85 4139 16 700829878H1 SOYMON019 g3021337 BLASTN 417 1e−52 86 4140 16 700671825H1 SOYMON006 g3021337 BLASTN 431 1e−52 79 4141 16 700755240H1 SOYMON014 g3021337 BLASTN 731 1e−52 88 4142 16 701011659H1 SOYMON019 g3021337 BLASTN 734 1e−52 86 4143 16 701011547H1 SOYMON019 g3021337 BLASTN 381 1e−51 84 4144 16 700835614H1 SOYMON019 g3021337 BLASTN 437 1e−51 80 4145 16 700671849H1 SOYMON006 g3021337 BLASTN 471 1e−51 87 4146 16 700734822H1 SOYMON010 g3021337 BLASTN 486 1e−51 79 4147 16 700830223H1 SOYMON019 g3021337 BLASTN 622 1e−51 84 4148 16 700659970H1 SOYMON004 g3021337 BLASTN 722 1e−51 82 4149 16 701101779H1 SOYMON028 g3021337 BLASTN 728 1e−51 86 4150 16 700852553H1 SOYMON023 g3021337 BLASTN 490 1e−50 88 4151 16 700853857H1 SOYMON023 g3021337 BLASTN 711 1e−50 88 4152 16 700980358H1 SOYMON009 g3021337 BLASTN 712 1e−50 85 4153 16 700672182H1 SOYMON006 g3021337 BLASTN 714 1e−50 89 4154 16 700748455H1 SOYMON013 g3021337 BLASTN 396 1e−49 85 4155 16 700657257H1 SOYMON004 g3021337 BLASTN 694 1e−49 75 4156 16 700729301H1 SOYMON009 g3021337 BLASTN 702 1e−49 80 4157 16 700726175H1 SOYMON009 g3021337 BLASTN 704 1e−49 80 4158 16 700966844H1 SOYMON028 g3021337 BLASTN 414 1e−47 81 4159 16 700960965H1 SOYMON022 g3021337 BLASTN 452 1e−47 85 4160 16 700678326H1 SOYMON007 g3021337 BLASTN 480 1e−47 83 4161 16 700751042H1 SOYMON014 g3021337 BLASTN 675 1e−47 87 4162 16 700830863H1 SOYMON019 g3021337 BLASTN 343 1e−46 84 4163 16 700870215H1 SOYMON016 g3021337 BLASTN 667 1e−46 80 4164 16 701213640H1 SOYMON035 g3021337 BLASTN 667 1e−46 87 4165 16 700658278H1 SOYMON004 g3021337 BLASTN 425 1e−44 87 4166 16 700942532H1 SOYMON024 g3021337 BLASTN 583 1e−44 83 4167 16 700986276H1 SOYMON009 g3021337 BLASTN 630 1e−43 81 4168 16 700870216H1 SOYMON016 g3021337 BLASTN 457 1e−42 82 4169 16 700899828H1 SOYMON027 g3021337 BLASTN 464 1e−42 83 4170 16 700678816H1 SOYMON007 g3021337 BLASTN 618 1e−42 86 4171 16 700666809H1 SOYMON005 g3021337 BLASTN 621 1e−42 82 4172 16 701098073H1 SOYMON028 g3021337 BLASTN 285 1e−41 83 4173 16 700669492H1 SOYMON006 g3021337 BLASTN 504 1e−39 83 4174 16 700975340H1 SOYMON009 g3021337 BLASTN 574 1e−39 81 4175 16 700753528H1 SOYMON014 g3021337 BLASTN 576 1e−39 81 4176 16 700665923H1 SOYMON005 g3021337 BLASTN 373 1e−35 84 4177 16 701038320H1 SOYMON029 g3021337 BLASTN 518 1e−34 84 4178 16 700755605H1 SOYMON014 g3021337 BLASTN 431 1e−33 81 4179 16 700890349H1 SOYMON024 g3021337 BLASTN 511 1e−33 88 4180 16 700669817H1 SOYMON006 g3021337 BLASTN 363 1e−31 87 4181 16 701097640H1 SOYMON028 g3021337 BLASTN 476 1e−30 67 4182 16 700562959H1 SOYMON002 g3021337 BLASTN 482 1e−30 81 4183 16 700852454H1 SOYMON023 g3021337 BLASTN 446 1e−28 77 4184 16 701121443H1 SOYMON037 g3021337 BLASTN 418 1e−24 84 4185 16 701118247H1 SOYMON037 g3021337 BLASTN 280 1e−18 85 4186 16 700665401H1 SOYMON005 g927505 BLASTX 172 1e−16 94 4187 16 700750038H1 SOYMON013 g3021338 BLASTX 162 1e−15 84 4188 16 700665414H1 SOYMON005 g3021337 BLASTN 273 1e−13 88 4189 16 700889072H1 SOYMON024 g3021338 BLASTX 136 1e−11 83 4190 16 700727964H1 SOYMON009 g927505 BLASTX 137 1e−11 86 4191 16 700680648H1 SOYMON008 g3021337 BLASTN 226 1e−10 73 4192 16 701044547H1 SOYMON032 g927505 BLASTX 91 1e−9 76 4193 16 700649174H1 SOYMON003 g3021338 BLASTX 126 1e−9 83 4194 16531 701120682H1 SOYMON037 g3021337 BLASTN 716 1e−50 77 4195 1701 700993909H1 SOYMON011 g22633 BLASTX 112 1e−31 78 4196 1701 700955490H1 SOYMON022 g22633 BLASTX 176 1e−25 70 4197 1701 700682081H1 SOYMON008 g22633 BLASTX 147 1e−20 68 4198 1701 700988843H1 SOYMON011 g22633 BLASTX 90 1e−14 67 4199 1701 700740531H1 SOYMON012 g22633 BLASTX 92 1e−12 64 4200 1701 700790059H2 SOYMON011 g22633 BLASTX 92 1e−12 67 4201 1701 700872670H1 SOYMON018 g169037 BLASTX 144 1e−12 90 4202 1701 700990591H1 SOYMON011 g22632 BLASTN 199 1e−11 68 4203 1701 700743120H1 SOYMON012 g22633 BLASTX 92 1e−9 68 4204 1701 700994931H1 SOYMON011 g22633 BLASTX 92 1e−8 64 4205 1938 700738074H1 SOYMON012 g927507 BLASTX 134 1e−11 90 4206 239 701126904H1 SOYMON037 g169037 BLASTX 231 1e−24 81 4207 239 700668532H1 SOYMON006 g169037 BLASTX 202 1e−20 83 4208 239 700666028H1 SOYMON005 g218155 BLASTX 186 1e−18 78 4209 239 701009915H2 SOYMON019 g169037 BLASTX 180 1e−17 84 4210 239 700943660H1 SOYMON024 g169037 BLASTX 180 1e−17 84 4211 239 701100047H2 SOYMON028 g169037 BLASTX 160 1e−15 84 4212 239 700794458H1 SOYMON017 g22633 BLASTX 131 1e−10 58 4213 239 700738441H1 SOYMON012 g169037 BLASTX 118 1e−8 78 4214 3425 700984050H1 SOYMON009 g3021337 BLASTN 874 1e−64 80 4215 3425 701014509H1 SOYMON019 g3021337 BLASTN 520 1e−60 80 4216 3425 701138819H1 SOYMON038 g3021337 BLASTN 815 1e−59 80 4217 3425 700977309H1 SOYMON009 g3021337 BLASTN 809 1e−58 80 4218 3425 700984876H1 SOYMON009 g3021337 BLASTN 813 1e−58 80 4219 3425 701046151H1 SOYMON032 g3021337 BLASTN 730 1e−52 80 4220 3425 700976571H1 SOYMON009 g3021337 BLASTN 737 1e−52 81 4221 3425 700889668H1 SOYMON024 g3021337 BLASTN 737 1e−52 81 4222 3425 701045371H1 SOYMON032 g3021337 BLASTN 716 1e−50 79 4223 3425 700548283H1 SOYMON002 g3021337 BLASTN 700 1e−49 81 4224 3425 701103461H1 SOYMON028 g3021337 BLASTN 705 1e−49 81 4225 3425 700898446H1 SOYMON027 g3021337 BLASTN 686 1e−48 83 4226 3425 701006432H1 SOYMON019 g3021337 BLASTN 688 1e−48 83 4227 3425 701041476H1 SOYMON029 g3021337 BLASTN 693 1e−48 81 4228 3425 700568335H1 SOYMON002 g3021337 BLASTN 678 1e−47 82 4229 3425 701046312H1 SOYMON032 g3021337 BLASTN 650 1e−45 85 4230 3425 701050171H1 SOYMON032 g3021337 BLASTN 650 1e−45 85 4231 3425 700685063H1 SOYMON008 g3021337 BLASTN 643 1e−44 83 4232 3425 701010250H2 SOYMON019 g3021337 BLASTN 542 1e−36 86 4233 3425 700665454H1 SOYMON005 g3021337 BLASTN 520 1e−34 80 4234 3425 701043888H1 SOYMON032 g3021337 BLASTN 495 1e−32 85 4235 3425 700726806H1 SOYMON009 g3021337 BLASTN 213 1e−23 76 4236 491 700997879H1 SOYMON018 g22632 BLASTN 789 1e−56 77 4237 491 700646208H1 SOYMON012 g22632 BLASTN 733 1e−52 76 4238 491 700559796H1 SOYMON001 g22632 BLASTN 715 1e−50 76 4239 491 700789784H1 SOYMON011 g22632 BLASTN 664 1e−46 76 4240 491 700683122H1 SOYMON008 g22632 BLASTN 485 1e−41 86 4241 491 701105914H1 SOYMON036 g22632 BLASTN 504 1e−41 73 4242 491 700558789H1 SOYMON001 g22632 BLASTN 607 1e−41 74 4243 491 700873051H1 SOYMON018 g22632 BLASTN 608 1e−41 75 4244 491 700684010H1 SOYMON008 g22632 BLASTN 597 1e−40 75 4245 491 700786096H2 SOYMON011 g22632 BLASTN 576 1e−39 75 4246 491 700731865H1 SOYMON010 g22632 BLASTN 582 1e−39 75 4247 491 701108111H1 SOYMON036 g22632 BLASTN 467 1e−38 75 4248 491 700740887H1 SOYMON012 g22632 BLASTN 567 1e−38 74 4249 491 700559579H1 SOYMON001 g22632 BLASTN 572 1e−38 75 4250 491 700996104H1 SOYMON018 g22632 BLASTN 476 1e−37 76 4251 491 700682145H1 SOYMON008 g22632 BLASTN 542 1e−36 74 4252 491 700737263H1 SOYMON010 g22632 BLASTN 526 1e−35 74 4253 491 700547963H1 SOYMON001 g22632 BLASTN 527 1e−35 73 4254 491 700686296H1 SOYMON008 g22632 BLASTN 527 1e−35 73 4255 491 700646072H1 SOYMON011 g22632 BLASTN 537 1e−35 74 4256 491 701106662H1 SOYMON036 g22632 BLASTN 514 1e−34 74 4257 491 700684335H1 SOYMON008 g22632 BLASTN 516 1e−34 74 4258 491 701000609H1 SOYMON018 g22632 BLASTN 520 1e−34 74 4259 491 700685658H1 SOYMON008 g22632 BLASTN 520 1e−34 74 4260 491 700875532H1 SOYMON018 g22632 BLASTN 521 1e−34 73 4261 491 700685813H1 SOYMON008 g22632 BLASTN 502 1e−33 74 4262 491 700872948H1 SOYMON018 g22632 BLASTN 502 1e−33 74 4263 491 700730264H1 SOYMON009 g22632 BLASTN 502 1e−33 74 4264 491 701104554H1 SOYMON036 g22632 BLASTN 503 1e−33 74 4265 491 700960601H1 SOYMON022 g22632 BLASTN 503 1e−33 74 4266 491 700876633H1 SOYMON018 g22632 BLASTN 503 1e−33 74 4267 491 700739662H1 SOYMON012 g22632 BLASTN 504 1e−33 72 4268 491 700685904H1 SOYMON008 g22632 BLASTN 505 1e−33 72 4269 491 700995183H1 SOYMON011 g22632 BLASTN 513 1e−33 73 4270 491 700901996H1 SOYMON027 g22632 BLASTN 513 1e−33 74 4271 491 700727070H1 SOYMON009 g22632 BLASTN 490 1e−32 72 4272 491 700685790H1 SOYMON008 g22632 BLASTN 492 1e−32 74 4273 491 700998652H1 SOYMON018 g22632 BLASTN 494 1e−32 72 4274 491 700740465H1 SOYMON012 g22632 BLASTN 482 1e−31 74 4275 491 700682621H2 SOYMON008 g22632 BLASTN 484 1e−31 74 4276 491 700874316H1 SOYMON018 g22632 BLASTN 466 1e−30 73 4277 491 700686477H1 SOYMON008 g22632 BLASTN 473 1e−30 73 4278 491 700739979H1 SOYMON012 g22632 BLASTN 476 1e−30 74 4279 491 700739416H1 SOYMON012 g22632 BLASTN 476 1e−30 74 4280 491 700685976H1 SOYMON008 g22632 BLASTN 476 1e−30 74 4281 491 700739629H1 SOYMON012 g22632 BLASTN 486 1e−30 70 4282 491 700989163H1 SOYMON011 g22632 BLASTN 468 1e−29 72 4283 491 701000555H1 SOYMON018 g22632 BLASTN 477 1e−29 72 4284 491 700872702H1 SOYMON018 g22632 BLASTN 436 1e−28 72 4285 491 701000781H1 SOYMON018 g22632 BLASTN 460 1e−28 73 4286 491 700682760H1 SOYMON008 g22632 BLASTN 463 1e−28 72 4287 491 700740390H1 SOYMON012 g22632 BLASTN 440 1e−27 73 4288 491 700685346H1 SOYMON008 g22632 BLASTN 451 1e−27 72 4289 491 700557272H1 SOYMON001 g22632 BLASTN 250 1e−26 78 4290 491 700953343H1 SOYMON022 g22632 BLASTN 349 1e−26 74 4291 491 700741960H1 SOYMON012 g22632 BLASTN 430 1e−26 73 4292 491 700680247H2 SOYMON008 g22632 BLASTN 425 1e−25 67 4293 491 700680002H2 SOYMON008 g22632 BLASTN 241 1e−24 72 4294 491 700684827H1 SOYMON008 g22632 BLASTN 379 1e−24 74 4295 491 700956353H1 SOYMON022 g22632 BLASTN 410 1e−24 72 4296 491 700787513H1 SOYMON011 g22632 BLASTN 235 1e−22 72 4297 491 700725070H1 SOYMON009 g22632 BLASTN 241 1e−22 71 4298 491 700741111H1 SOYMON012 g22632 BLASTN 304 1e−22 73 4299 491 700738230H1 SOYMON012 g22632 BLASTN 241 1e−21 72 4300 491 700985308H1 SOYMON009 g22632 BLASTN 241 1e−21 80 4301 491 700991396H1 SOYMON011 g22632 BLASTN 350 1e−21 72 4302 491 700741276H1 SOYMON012 g22632 BLASTN 379 1e−21 71 4303 491 700740223H1 SOYMON012 g22632 BLASTN 241 1e−20 72 4304 491 700738808H1 SOYMON012 g22632 BLASTN 241 1e−20 72 4305 491 700997995H1 SOYMON018 g22632 BLASTN 241 1e−19 81 4306 491 700989713H1 SOYMON011 g22632 BLASTN 241 1e−19 73 4307 491 700875139H1 SOYMON018 g22632 BLASTN 241 1e−19 71 4308 491 700958366H1 SOYMON022 g22632 BLASTN 241 1e−18 71 4309 491 700683887H1 SOYMON008 g22632 BLASTN 344 1e−18 70 4310 491 700740788H1 SOYMON012 g22632 BLASTN 339 1e−17 70 4311 491 700743058H1 SOYMON012 g22632 BLASTN 205 1e−16 81 4312 491 700996423H1 SOYMON018 g22632 BLASTN 234 1e−16 80 4313 491 700686075H1 SOYMON008 g22632 BLASTN 241 1e−16 71 4314 491 700738811H1 SOYMON012 g22632 BLASTN 193 1e−15 72 4315 491 700998312H1 SOYMON018 g22632 BLASTN 234 1e−15 73 4316 491 700681825H1 SOYMON008 g22632 BLASTN 241 1e−15 81 4317 491 701109105H1 SOYMON036 g22632 BLASTN 290 1e−14 69 4318 491 701203741H2 SOYMON035 g22632 BLASTN 230 1e−13 78 4319 491 700740785H1 SOYMON012 g22632 BLASTN 287 1e−13 68 4320 491 700738486H1 SOYMON012 g22632 BLASTN 295 1e−13 64 4321 491 700739078H1 SOYMON012 g22632 BLASTN 178 1e−12 73 4322 491 701002287H1 SOYMON018 g22632 BLASTN 255 1e−12 74 4323 491 700742470H1 SOYMON012 g22632 BLASTN 278 1e−12 69 4324 491 700743421H1 SOYMON012 g22632 BLASTN 261 1e−11 71 4325 491 700744039H1 SOYMON012 g22632 BLASTN 265 1e−11 69 4326 491 700789444H2 SOYMON011 g22632 BLASTN 158 1e−10 87 4327 491 700741074H1 SOYMON012 g22632 BLASTN 178 1e−10 77 4328 491 700998877H1 SOYMON018 g22632 BLASTN 235 1e−10 72 4329 491 700740005H1 SOYMON012 g22633 BLASTX 75 1e−9 64 4330 491 700872703H1 SOYMON018 g169037 BLASTX 116 1e−9 83 4331 491 700990557H1 SOYMON011 g22632 BLASTN 241 1e−9 76 4332 491 701001909H1 SOYMON018 g22632 BLASTN 241 1e−9 76 4333 491 700875039H1 SOYMON018 g22632 BLASTN 241 1e−9 72 4334 491 700743495H1 SOYMON012 g22632 BLASTN 241 1e−9 76 4335 491 700743995H1 SOYMON012 g22632 BLASTN 241 1e−9 76 4336 491 700743301H1 SOYMON012 g22632 BLASTN 241 1e−9 76 4337 491 700742515H1 SOYMON012 g22632 BLASTN 241 1e−9 76 4338 491 701001445H1 SOYMON018 g169037 BLASTX 115 1e−8 92 4339 491 700554881H1 SOYMON001 g169037 BLASTX 116 1e−8 94 4340 491 700954194H1 SOYMON022 g169037 BLASTX 116 1e−8 94 4341 491 700996869H1 SOYMON018 g22632 BLASTN 230 1e−8 76 4342 491 700897820H1 SOYMON027 g22632 BLASTN 234 1e−8 74 4343 491 700742574H1 SOYMON012 g22632 BLASTN 234 1e−8 74 4344 491 700684738H1 SOYMON008 g22632 BLASTN 235 1e−8 75 4345 7368 700739343H1 SOYMON012 g927507 BLASTX 164 1e−15 88 4346 -GM32379 LIB3051-015- LIB3051 g3021337 BLASTN 260 1e−28 77 Q1-E1-B12 4347 -GM8265 LIB3039-048- LIB3039 g3021337 BLASTN 481 1e−29 65 Q1-E1-F11 4348 16 LIB3027-010- LIB3027 g3021337 BLASTN 1393 1e−107 82 Q1-B1-B7 4349 16 LIB3039-049- LIB3039 g3021337 BLASTN 1297 1e−99 83 Q1-E1-B8 4350 16 LIB3051-061- LIB3051 g3021337 BLASTN 1303 1e−99 84 Q1-K1-E11 4351 16 LIB3056-009- LIB3056 g3021337 BLASTN 1126 1e−96 84 Q1-N1-A10 4352 16 LIB3051-025- LIB3051 g3021337 BLASTN 1262 1e−96 83 Q1-K1-E11 4353 16 LIB3056-014- LIB3056 g3021337 BLASTN 1077 1e−94 81 Q1-N1-E1 4354 16 LIB3055-005- LIB3055 g3021337 BLASTN 1227 1e−93 84 Q1-N1-A8 4355 16 LIB3040-045- LIB3040 g3021337 BLASTN 1211 1e−92 83 Q1-E1-A4 4356 16 LIB3028-010- LIB3028 g3021337 BLASTN 1215 1e−92 83 Q1-B1-G9 4357 16 LIB3056-010- LIB3056 g3021337 BLASTN 1217 1e−92 84 Q1-N1-G8 4358 16 LIB3039-029- LIB3039 g3021337 BLASTN 1128 1e−85 85 Q1-E1-A6 4359 16 LIB3051-014- LIB3051 g3021337 BLASTN 716 1e−80 83 Q1-E1-D2 4360 16 LIB3030-010- LIB3030 g3021337 BLASTN 1052 1e−78 83 Q1-B1-D7 4361 16 LIB3051-094- LIB3051 g3021337 BLASTN 778 1e−74 83 Q1-K1-A9 4362 16 LIB3028-030- LIB3028 g3021337 BLASTN 953 1e−70 85 Q1-B1-C9 4363 16 LIB3052-004- LIB3052 g3021337 BLASTN 868 1e−63 82 Q1-N1-D8 4364 16 LIB3065-014- LIB3065 g3021337 BLASTN 540 1e−61 79 Q1-N1-A3 4365 16 LIB3050-019- LIB3050 g168420 BLASTX 223 1e−40 63 Q1-K1-H1 4366 16 LIB3051-062- LIB3051 g3021337 BLASTN 541 1e−38 79 Q1-K1-B5 4367 3425 LIB3051-067- LIB3051 g3021337 BLASTN 1082 1e−81 78 Q1-K1-E7 4368 3425 LIB3050-006- LIB3050 g3021337 BLASTN 752 1e−57 75 Q1-E1-G7 4369 491 LIB3028-011- LIB3028 g22632 BLASTN 911 1e−67 75 Q1-B1-B9 4370 491 LIB3028-011- LIB3028 g22632 BLASTN 886 1e−65 77 Q1-B1-F2 MAIZE FRUCTOSE-1,6-BISPHOSPHATASE 4371 -700262935 700262935H1 SATMON017 g3041775 BLASTX 184 1e−18 94 4372 -700432173 700432173H1 SATMONN01 g1790679 BLASTX 123 1e−16 56 4373 -700455709 700455709H1 SATMON029 g3041776 BLASTN 597 1e−40 85 4374 -700573083 700573083H1 SATMON030 g3041775 BLASTX 69 1e−10 64 4375 -701158577 701158577H1 SATMONN04 g895908 BLASTN 200 1e−10 84 4376 12846 700101851H1 SATMON009 g3041776 BLASTN 1312 1e−100 91 4377 12846 700101541H1 SATMON009 g3041776 BLASTN 1252 1e−95 90 4378 12846 700581510H1 SATMON031 g3041776 BLASTN 872 1e−82 90 4379 15627 700046054H1 SATMON004 g21736 BLASTN 1213 1e−92 91 4380 15627 700421605H1 SATMONN01 g3041776 BLASTN 664 1e−77 90 4381 15627 700445495H1 SATMON027 g21736 BLASTN 1004 1e−74 84 4382 15627 700042188H1 SATMON004 g3041776 BLASTN 875 1e−64 88 4383 16870 700100752H1 SATMON009 g3041776 BLASTN 257 1e−33 75 4384 16870 700044805H1 SATMON004 g3041776 BLASTN 194 1e−14 76 4385 16870 700099217H1 SATMON009 g21736 BLASTN 246 1e−9 59 4386 25562 701166271H1 SATMONN04 g895908 BLASTN 352 1e−43 91 4387 25562 701163676H1 SATMONN04 g895908 BLASTN 299 1e−37 91 4388 32637 700097620H1 SATMON009 g895908 BLASTN 1380 1e−106 92 4389 32637 700580175H1 SATMON031 g895908 BLASTN 930 1e−68 89 4390 5480 700098780H1 SATMON009 g895908 BLASTN 1103 1e−90 95 4391 5480 700043335H1 SATMON004 g895908 BLASTN 1026 1e−76 93 4392 5480 700043111H1 SATMON004 g895908 BLASTN 879 1e−64 97 4393 5480 700442189H1 SATMON026 g3041774 BLASTN 536 1e−54 93 4394 5480 700208394H1 SATMON016 g895908 BLASTN 520 1e−43 92 4395 5480 700045530H1 SATMON004 g895908 BLASTN 613 1e−42 97 4396 5480 700098393H1 SATMON009 g895908 BLASTN 308 1e−16 88 4397 8243 700264654H1 SATMON017 g3041774 BLASTN 942 1e−69 84 4398 8243 700479624H1 SATMON034 g3041774 BLASTN 902 1e−66 82 4399 8243 700448974H1 SATMON028 g3041774 BLASTN 876 1e−64 84 4400 8666 700100948H1 SATMON009 g895908 BLASTN 1327 1e−101 92 4401 8666 700212964H1 SATMON016 g895908 BLASTN 1189 1e−90 91 4402 8666 700578027H1 SATMON031 g895908 BLASTN 1076 1e−80 91 4403 -L1485381 LIB148-057- LIB148 g440591 BLASTX 80 1e−30 63 Q1-E1-E6 4404 -L30662838 LIB3066-032- LIB3066 g895908 BLASTN 640 1e−58 86 Q1-K1-F11 4405 -L30662839 LIB3066-035- LIB3066 g3041774 BLASTN 215 1e−15 77 Q1-K1-F11 4406 -L362913 LIB36-013- LIB36 g3041776 BLASTN 937 1e−69 88 Q1-E1-D10 4407 -L831319 LIB83-003- LIB83 g895908 BLASTN 341 1e−58 86 Q1-E1-B4 4408 -L832444 LIB83-005- LIB83 g3041776 BLASTN 575 1e−37 93 Q1-E1-D2 4409 -L841984 LIB84-023- LIB84 g895908 BLASTN 937 1e−69 82 Q1-E1-F10 4410 12846 LIB83-008- LIB83 g3041776 BLASTN 1610 1e−135 92 Q1-E1-A8 4411 12846 LIB3078-003- LIB3078 g3041776 BLASTN 873 1e−98 93 Q1-K1-C7 4412 16870 LIB3060-052- LIB3060 g21736 BLASTN 377 1e−66 70 Q1-K1-D11 4413 26002 LIB83-008- LIB83 g3041776 BLASTN 378 1e−20 86 Q1-E1-B10 4414 32637 LIB189-010- LIB189 g895908 BLASTN 1182 1e−138 92 Q1-E1-C10 4415 5480 LIB83-002- LIB83 g895908 BLASTN 1773 1e−139 94 Q1-E1-C2 4416 5480 LIB36-016- LIB36 g895908 BLASTN 1615 1e−125 94 Q2-E2-H10 4417 5480 LIB189-032- LIB189 g895908 BLASTN 1598 1e−124 95 Q1-E1-B6 4418 5480 LIB36-010- LIB36 g895908 BLASTN 1574 1e−122 93 Q1-E1-C4 4419 5480 LIB3060-010- LIB3060 g895908 BLASTN 990 1e−82 91 Q1-K1-D2 4420 5480 LIB189-021- LIB189 g895908 BLASTN 1045 1e−78 93 Q1-E1-E10 4421 5480 LIB84-013- LIB84 g895908 BLASTN 1032 1e−77 96 Q1-E1-F7 SOYBEAN FRUCTOSE-1,6-BISPHOSPHATASE 4422 -700685384 700685384H1 SOYMON008 g21244 BLASTN 597 1e−49 80 4423 -700737915 700737915H1 SOYMON012 g515746 BLASTN 1316 1e−100 97 4424 -700741457 700741457H1 SOYMON012 g3041774 BLASTN 692 1e−58 80 4425 -700873234 700873234H1 SOYMON018 g166955 BLASTN 417 1e−33 83 4426 -700874831 700874831H1 SOYMON018 g515746 BLASTN 1295 1e−99 100 4427 -700983024 700983024H1 SOYMON009 g166955 BLASTN 575 1e−60 76 4428 -700993304 700993304H1 SOYMON011 g166955 BLASTN 902 1e−66 84 4429 -700996155 700996155H1 SOYMON018 g3041774 BLASTN 651 1e−45 83 4430 -700996632 700996632H1 SOYMON018 g515746 BLASTN 507 1e−51 90 4431 -700998027 700998027H1 SOYMON018 g515746 BLASTN 636 1e−65 94 4432 -701209548 701209548H1 SOYMON035 g3041774 BLASTN 642 1e−44 83 4433 10129 700870828H1 SOYMON018 g21244 BLASTN 827 1e−60 79 4434 10129 700741669H1 SOYMON012 g21244 BLASTN 657 1e−53 80 4435 10348 700555754H1 SOYMON001 g21244 BLASTN 466 1e−29 77 4436 10348 700991527H1 SOYMON011 g440591 BLASTX 169 1e−16 88 4437 13716 700898719H1 SOYMON027 g515746 BLASTN 1186 1e−90 97 4438 13716 700993540H1 SOYMON011 g515746 BLASTN 1179 1e−89 98 4439 13716 700909657H1 SOYMON022 g515746 BLASTN 568 1e−57 86 4440 1894 700555054H1 SOYMON001 g515746 BLASTN 1320 1e−101 100 4441 1894 700685264H1 SOYMON008 g515746 BLASTN 1323 1e−101 99 4442 1894 700558854H1 SOYMON001 g515746 BLASTN 695 1e−98 100 4443 1894 700554755H1 SOYMON001 g515746 BLASTN 767 1e−98 99 4444 1894 701000504H1 SOYMON018 g515746 BLASTN 626 1e−95 98 4445 1894 700738115H1 SOYMON012 g515746 BLASTN 1230 1e−93 100 4446 1894 700992933H1 SOYMON011 g515746 BLASTN 1074 1e−91 98 4447 1894 701107444H1 SOYMON036 g515746 BLASTN 1201 1e−91 99 4448 1894 700852823H1 SOYMON023 g515746 BLASTN 1041 1e−90 98 4449 1894 700733478H1 SOYMON010 g515746 BLASTN 1150 1e−90 97 4450 1894 701105185H1 SOYMON036 g515746 BLASTN 641 1e−87 89 4451 1894 700737830H1 SOYMON012 g515746 BLASTN 1060 1e−87 100 4452 1894 700685110H1 SOYMON008 g515746 BLASTN 597 1e−86 90 4453 1894 700968307H1 SOYMON036 g515746 BLASTN 1113 1e−84 97 4454 1894 700653014H1 SOYMON003 g515746 BLASTN 587 1e−82 90 4455 1894 700555504H1 SOYMON001 g515746 BLASTN 626 1e−81 88 4456 1894 700751540H1 SOYMON014 g515746 BLASTN 585 1e−77 91 4457 1894 700901976H1 SOYMON027 g515746 BLASTN 505 1e−73 87 4458 1894 700986496H1 SOYMON009 g515746 BLASTN 559 1e−73 90 4459 1894 700751580H1 SOYMON014 g515746 BLASTN 569 1e−72 89 4460 1894 700751532H1 SOYMON014 g515746 BLASTN 571 1e−72 90 4461 1894 700990937H1 SOYMON011 g515746 BLASTN 544 1e−71 88 4462 1894 700740789H1 SOYMON012 g515746 BLASTN 630 1e−69 100 4463 1894 700743994H1 SOYMON012 g515746 BLASTN 945 1e−69 100 4464 1894 700754374H1 SOYMON014 g515746 BLASTN 460 1e−62 91 4465 1894 701001295H1 SOYMON018 g515746 BLASTN 541 1e−62 97 4466 1894 701155952H1 SOYMON031 g515746 BLASTN 568 1e−51 83 4467 1894 700872212H1 SOYMON018 g515746 BLASTN 670 1e−47 100 4468 1894 700682196H1 SOYMON008 g515746 BLASTN 609 1e−41 98 4469 1894 700738779H1 SOYMON012 g515746 BLASTN 252 1e−16 82 4470 26568 700844816H1 SOYMON021 g21244 BLASTN 649 1e−45 78 4471 27512 701128049H1 SOYMON037 g440591 BLASTX 185 1e−18 87 4472 27512 701152064H1 SOYMON031 g895908 BLASTN 243 1e−9 77 4473 7128 700649626H1 SOYMON003 g166955 BLASTN 326 1e−25 79 4474 7128 700649846H1 SOYMON003 g440591 BLASTX 125 1e−15 81 4475 10348 LIB3030-010- LIB3030 g21244 BLASTN 476 1e−28 76 Q1-B1-C7 MAIZE TRANSKETOLASE 4476 -700097383 700097383H1 SATMON009 g664902 BLASTN 1029 1e−76 80 4477 -701159054 701159054H1 SATMONN04 g2529342 BLASTX 214 1e−27 79 4478 -701184582 701184582H1 SATMONN06 g1658321 BLASTN 745 1e−53 74 4479 1244 700553205H1 SATMON022 g1658321 BLASTN 816 1e−59 75 4480 1244 700473792H1 SATMON025 g1658321 BLASTN 826 1e−59 75 4481 1244 700405168H1 SATMON028 g1658321 BLASTN 805 1e−58 75 4482 1244 700089307H1 SATMON011 g1658321 BLASTN 743 1e−53 74 4483 1244 700355533H1 SATMON024 g1658321 BLASTN 589 1e−51 76 4484 1244 700085136H1 SATMON011 g1658321 BLASTN 690 1e−48 76 4485 1244 700382850H1 SATMON024 g664900 BLASTN 537 1e−47 72 4486 1244 700454437H1 SATMON029 g1658321 BLASTN 655 1e−45 75 4487 1244 700150022H1 SATMON007 g1658321 BLASTN 606 1e−41 76 4488 1244 700212701H1 SATMON016 g1658321 BLASTN 507 1e−40 74 4489 1244 700438654H1 SATMON026 g2529342 BLASTX 160 1e−24 89 4490 1244 700458530H1 SATMON029 g2529342 BLASTX 177 1e−20 87 4491 2946 700262031H1 SATMON017 g1658321 BLASTN 467 1e−30 74 4492 3403 700075930H1 SATMON007 g664900 BLASTN 968 1e−71 81 4493 3403 700381012H1 SATMON023 g1658321 BLASTN 949 1e−70 80 4494 3403 700243701H1 SATMON010 g1658321 BLASTN 874 1e−63 80 4495 3403 700220485H1 SATMON011 g664900 BLASTN 666 1e−54 74 4496 3403 700045165H1 SATMON004 g664900 BLASTN 734 1e−52 73 4497 3403 701185190H1 SATMONN06 g664900 BLASTN 709 1e−50 77 4498 3403 700552475H1 SATMON022 g664900 BLASTN 591 1e−49 81 4499 3403 700044755H1 SATMON004 g664900 BLASTN 690 1e−48 72 4500 3403 700051910H1 SATMON003 g664900 BLASTN 671 1e−47 77 4501 3403 700027425H1 SATMON003 g664900 BLASTN 675 1e−47 71 4502 3403 700048347H1 SATMON003 g664900 BLASTN 662 1e−46 71 4503 3403 700380608H1 SATMON021 g1658321 BLASTN 623 1e−43 82 4504 3403 700448484H1 SATMON027 g664900 BLASTN 522 1e−33 71 4505 3403 700184906H1 SATMON014 g2529342 BLASTX 251 1e−27 77 4506 3403 700048819H1 SATMON003 g664900 BLASTN 453 1e−27 74 4507 3403 701167994H1 SATMONN05 g2529342 BLASTX 193 1e−19 76 4508 8097 700084375H1 SATMON011 g664900 BLASTN 855 1e−76 79 4509 8097 700445226H1 SATMON027 g664900 BLASTN 464 1e−60 79 4510 8097 700240770H1 SATMON010 g664900 BLASTN 750 1e−60 80 4511 8097 700045122H1 SATMON004 g664900 BLASTN 638 1e−54 80 4512 3403 LIB3060-013- LIB3060 g664900 BLASTN 1052 1e−78 72 Q1-K1-A12 4513 3403 LIB3078-007- LIB3078 g664900 BLASTN 629 1e−41 69 Q1-K1-G3 MAIZE PUTATIVE TRANSKETOLASE 4514 -700045462 700045462H1 SATMON004 g2612940 BLASTN 1219 1e−92 89 4515 -700223919 700223919H1 SATMON011 g2612940 BLASTN 1025 1e−76 87 4516 -700256830 700256830H1 SATMON017 g2612940 BLASTN 1029 1e−76 87 4517 -701169515 701169515H1 SATMONN05 g2612940 BLASTN 327 1e−40 92 4518 23377 700263420H1 SATMON017 g2612940 BLASTN 489 1e−31 75 4519 23377 701185311H1 SATMONN06 g2612940 BLASTN 460 1e−27 78 4520 7446 700624329H1 SATMON034 g2612940 BLASTN 1046 1e−87 88 4521 7446 700159091H1 SATMON012 g2612940 BLASTN 898 1e−77 89 4522 -L30626416 LIB3062-048- LIB3062 g2612940 BLASTN 808 1e−74 86 Q1-K1-D12 4523 -L30684293 LIB3068-046- LIB3068 g2612940 BLASTN 846 1e−90 87 Q1-K1-B2 4524 28081 LIB36-007- LIB36 g2612940 BLASTN 521 1e−32 92 Q1-E1-F12 SOYBEAN TRANSKETOLASE 4525 -700646481 700646481H1 SOYMON013 g1658321 BLASTN 967 1e−71 83 4526 -700734535 700734535H1 SOYMON010 g1658321 BLASTN 822 1e−59 82 4527 -700865886 700865886H1 SOYMON016 g1658321 BLASTN 568 1e−38 82 4528 -700943688 700943688H1 SOYMON024 g1658321 BLASTN 902 1e−66 82 4529 -700954594 700954594H1 SOYMON022 g2529342 BLASTX 172 1e−16 75 4530 -701064360 701064360H1 SOYMON034 g664901 BLASTX 179 1e−17 80 4531 1039 700662776H1 SOYMON005 g1658321 BLASTN 755 1e−78 83 4532 1039 700663764H1 SOYMON005 g1658321 BLASTN 839 1e−61 82 4533 1039 700952282H1 SOYMON022 g1658321 BLASTN 785 1e−56 81 4534 1039 700835426H1 SOYMON019 g1658321 BLASTN 748 1e−53 81 4535 1039 700738038H1 SOYMON012 g1658321 BLASTN 559 1e−37 80 4536 1040 700606230H1 SOYMON008 g1658321 BLASTN 532 1e−69 82 4537 1040 700681196H2 SOYMON008 g1658321 BLASTN 866 1e−63 80 4538 1040 700876408H1 SOYMON018 g1658321 BLASTN 475 1e−60 82 4539 1040 700901259H1 SOYMON027 g1658321 BLASTN 821 1e−59 81 4540 1040 700996991H1 SOYMON018 g1658321 BLASTN 450 1e−58 80 4541 1040 700876984H1 SOYMON018 g1658321 BLASTN 807 1e−58 81 4542 1040 700871885H1 SOYMON018 g1658321 BLASTN 812 1e−58 81 4543 1040 700740158H1 SOYMON012 g1658321 BLASTN 767 1e−55 78 4544 1040 700787592H1 SOYMON011 g1658321 BLASTN 770 1e−55 80 4545 1040 700789355H2 SOYMON011 g1658321 BLASTN 727 1e−51 81 4546 1040 700786173H2 SOYMON011 g1658321 BLASTN 523 1e−47 79 4547 1040 700987027H1 SOYMON009 g1658321 BLASTN 680 1e−47 78 4548 1040 700683335H1 SOYMON008 g1658321 BLASTN 567 1e−38 80 4549 1040 700742402H1 SOYMON012 g1658321 BLASTN 521 1e−34 78 4550 1040 700682934H1 SOYMON008 g1658322 BLASTX 111 1e−22 79 4551 1040 701001535H1 SOYMON018 g664900 BLASTN 337 1e−18 85 4552 1381 701002017H1 SOYMON018 g1658321 BLASTN 860 1e−62 81 4553 1381 700680946H1 SOYMON008 g1658321 BLASTN 848 1e−61 75 4554 1381 700785920H2 SOYMON011 g1658321 BLASTN 715 1e−60 80 4555 1381 700741325H1 SOYMON012 g1658321 BLASTN 836 1e−60 81 4556 1381 700737257H1 SOYMON010 g1658321 BLASTN 783 1e−56 83 4557 1381 700743637H1 SOYMON012 g1658321 BLASTN 456 1e−47 79 4558 1381 700683536H1 SOYMON008 g1658321 BLASTN 682 1e−47 82 4559 1381 700899577H1 SOYMON027 g1658321 BLASTN 632 1e−43 73 4560 1381 700655539H1 SOYMON004 g1658321 BLASTN 399 1e−32 77 4561 1381 700743117H1 SOYMON012 g664901 BLASTX 144 1e−12 88 4562 1381 701047167H1 SOYMON032 g1658321 BLASTN 147 1e−10 88 4563 1694 700557862H1 SOYMON001 g1658321 BLASTN 918 1e−67 81 4564 1694 701124388H1 SOYMON037 g1658321 BLASTN 884 1e−64 84 4565 1694 700977906H1 SOYMON009 g1658321 BLASTN 741 1e−60 81 4566 1694 700741633H1 SOYMON012 g1658321 BLASTN 753 1e−60 83 4567 20534 701214424H1 SOYMON035 g1658321 BLASTN 855 1e−62 80 4568 20534 701214345H1 SOYMON035 g1658321 BLASTN 845 1e−61 81 4569 20534 700737144H1 SOYMON010 g1658321 BLASTN 743 1e−53 79 4570 20534 700737045H1 SOYMON010 g1658321 BLASTN 716 1e−50 80 4571 2081 700684191H1 SOYMON008 g1658321 BLASTN 243 1e−11 68 4572 2081 700871634H1 SOYMON018 g1658321 BLASTN 243 1e−9 65 4573 2081 700896859H1 SOYMON027 g1658321 BLASTN 243 1e−9 65 4574 2081 700741968H1 SOYMON012 g1658321 BLASTN 243 1e−9 65 4575 2081 700743285H1 SOYMON012 g1658321 BLASTN 234 1e−8 65 4576 2081 701105794H1 SOYMON036 g1658321 BLASTN 236 1e−8 65 4577 2081 700646243H1 SOYMON012 g1658321 BLASTN 236 1e−8 65 4578 2081 701104160H1 SOYMON036 g1658321 BLASTN 236 1e−8 65 4579 2081 700741863H1 SOYMON012 g1658321 BLASTN 238 1e−8 65 4580 2091 700651076H1 SOYMON003 g1658321 BLASTN 1055 1e−79 79 4581 2091 700874803H1 SOYMON018 g1658321 BLASTN 888 1e−65 82 4582 2091 700988611H1 SOYMON009 g1658321 BLASTN 419 1e−61 79 4583 2091 700657810H1 SOYMON004 g1658321 BLASTN 805 1e−58 81 4584 2091 700739094H1 SOYMON012 g1658321 BLASTN 425 1e−54 82 4585 2091 700962626H1 SOYMON022 g1658321 BLASTN 742 1e−52 78 4586 2091 700990046H1 SOYMON011 g1658321 BLASTN 376 1e−34 79 4587 3782 700870543H1 SOYMON018 g1658322 BLASTX 157 1e−25 68 4588 4096 700556949H1 SOYMON001 g664901 BLASTX 188 1e−18 92 4589 4096 700877014H1 SOYMON018 g664901 BLASTX 188 1e−18 92 4590 4096 700877022H1 SOYMON018 g664901 BLASTX 188 1e−18 92 4591 4096 700999039H1 SOYMON018 g664901 BLASTX 169 1e−16 91 4592 7870 700998419H1 SOYMON018 g1658321 BLASTN 430 1e−51 80 4593 7870 700557019H1 SOYMON001 g1658321 BLASTN 685 1e−48 80 4594 7870 700786020H2 SOYMON011 g1658321 BLASTN 531 1e−41 78 4595 7870 700740475H1 SOYMON012 g1658321 BLASTN 609 1e−41 74 4596 7870 700875020H1 SOYMON018 g1658321 BLASTN 525 1e−34 79 4597 7870 700674249H1 SOYMON007 g1658321 BLASTN 510 1e−33 82 4598 7870 700658256H1 SOYMON004 g2529342 BLASTX 178 1e−22 61 4599 7870 700677401H1 SOYMON007 g664901 BLASTX 158 1e−14 91 4600 9031 700874020H1 SOYMON018 g1658321 BLASTN 789 1e−56 79 4601 9031 700726463H1 SOYMON009 g1658321 BLASTN 758 1e−54 76 4602 9031 700869017H1 SOYMON016 g664900 BLASTN 743 1e−53 77 4603 9031 700566216H1 SOYMON002 g664901 BLASTX 201 1e−20 92 4604 1039 LIB3051-053- LIB3051 g1658321 BLASTN 1326 1e−101 80 Q1-K2-F1 4605 9031 LIB3039-045- LIB3039 g1658321 BLASTN 1033 1e−77 79 Q1-E1-D1 SOYBEAN PUTATIVE TRANSKETOLASE 4606 19183 700907766H1 SOYMON022 g2612940 BLASTN 395 1e−30 68 4607 -700764341 700764341H1 SOYMON021 g2612941 BLASTX 247 1e−39 75 4608 -700888745 700888745H1 SOYMON024 g2612941 BLASTX 237 1e−27 76 4609 -700909473 700909473H1 SOYMON022 g2612941 BLASTX 114 1e−16 53 4610 7224 700681472H2 SOYMON008 g2612941 BLASTX 107 1e−12 72 4611 19325 700751059H1 SOYMON014 g2244912 BLASTX 160 1e−15 78 4612 -GM40396 LIB3051-093- LIB3051 g2612941 BLASTX 246 1e−73 90 Q1-K1-D2 MAIZE SEDOHEPTULOSE-1,7-BISPHOSPHATASE 4613 1006 700423931H1 SATMONN01 g14265 BLASTX 128 1e−14 86 4614 29810 LIB36-010- LIB36 g2529375 BLASTN 911 1e−67 69 Q1-E1-H12 SOYBEAN SEDOHEPTULOSE-1,7-BISPHOSPHATASE 4615 -700895707 700895707H1 SOYMON027 g2529375 BLASTN 696 1e−49 74 4616 24265 701154827H1 SOYMON031 g2529375 BLASTN 893 1e−65 83 4617 24265 701157439H1 SOYMON031 g2529375 BLASTN 851 1e−62 83 4618 3027 700988602H1 SOYMON009 g2529375 BLASTN 911 1e−67 77 4619 3027 701001010H1 SOYMON018 g2529375 BLASTN 915 1e−67 79 4620 3027 700997516H1 SOYMON018 g2529375 BLASTN 504 1e−60 80 4621 3027 700788686H1 SOYMON011 g2529375 BLASTN 837 1e−60 79 4622 3027 700556469H1 SOYMON001 g2529375 BLASTN 816 1e−59 76 4623 3027 700999494H1 SOYMON018 g2529375 BLASTN 806 1e−58 76 4624 3027 701106923H1 SOYMON036 g2529375 BLASTN 812 1e−58 78 4625 3027 700557386H1 SOYMON001 g2529375 BLASTN 473 1e−57 78 4626 3027 700996203H1 SOYMON018 g2529375 BLASTN 787 1e−56 79 4627 3027 700951860H1 SOYMON022 g2529375 BLASTN 771 1e−55 76 4628 3027 700683415H1 SOYMON008 g2529375 BLASTN 762 1e−54 79 4629 3027 700872306H1 SOYMON018 g2529375 BLASTN 734 1e−52 78 4630 3027 700876576H1 SOYMON018 g2529375 BLASTN 739 1e−52 79 4631 3027 700876860H1 SOYMON018 g2529375 BLASTN 741 1e−52 78 4632 3027 700874809H1 SOYMON018 g2529375 BLASTN 426 1e−50 76 4633 3027 700992772H1 SOYMON011 g2529375 BLASTN 707 1e−50 79 4634 3027 700740276H1 SOYMON012 g2529375 BLASTN 700 1e−49 76 4635 3027 700876171H1 SOYMON018 g786465 BLASTN 454 1e−47 80 4636 3027 700557859H1 SOYMON001 g2529375 BLASTN 633 1e−43 71 4637 3027 700556904H1 SOYMON001 g2529375 BLASTN 523 1e−42 70 4638 3027 701124349H1 SOYMON037 g2529375 BLASTN 565 1e−38 74 4639 3027 700554878H1 SOYMON001 g2529375 BLASTN 390 1e−36 68 4640 3027 700556561H1 SOYMON001 g2529375 BLASTN 540 1e−36 66 4641 3027 701001629H1 SOYMON018 g2529375 BLASTN 517 1e−34 66 4642 3027 700789624H2 SOYMON011 g2529375 BLASTN 507 1e−33 66 4643 3027 700993071H1 SOYMON011 g2529375 BLASTN 511 1e−33 66 4644 3027 700556185H1 SOYMON001 g2529375 BLASTN 513 1e−33 66 4645 3027 700554166H1 SOYMON001 g2529375 BLASTN 520 1e−33 66 4646 3027 700680116H2 SOYMON008 g2529375 BLASTN 486 1e−31 65 4647 3027 700557591H1 SOYMON001 g2529375 BLASTN 497 1e−31 66 4648 3027 701108330H1 SOYMON036 g2529375 BLASTN 486 1e−30 65 4649 3027 700875128H1 SOYMON018 g2529375 BLASTN 460 1e−29 65 4650 3027 700991275H1 SOYMON011 g2529375 BLASTN 462 1e−29 64 4651 3027 700556249H1 SOYMON001 g2529375 BLASTN 466 1e−28 65 4652 3027 700559069H1 SOYMON001 g2529375 BLASTN 467 1e−28 72 4653 3027 700990985H1 SOYMON011 g2529375 BLASTN 444 1e−27 62 4654 3027 701062648H1 SOYMON033 g2529375 BLASTN 438 1e−26 64 4655 3027 700560603H1 SOYMON001 g2529375 BLASTN 441 1e−26 73 4656 3027 701109375H1 SOYMON036 g2529376 BLASTX 128 1e−23 59 4657 3027 700787023H2 SOYMON011 g2529376 BLASTX 158 1e−21 55 4658 3027 701053814H1 SOYMON032 g2529376 BLASTX 127 1e−19 52 4659 3027 701103839H1 SOYMON036 g2529376 BLASTX 162 1e−17 60 4660 3027 700874009H1 SOYMON018 g2529376 BLASTX 180 1e−17 50 4661 3027 700557201H1 SOYMON001 g14265 BLASTX 154 1e−16 70 4662 3027 701001319H1 SOYMON018 g2529375 BLASTN 324 1e−16 59 4663 3027 701105211H1 SOYMON036 g2529376 BLASTX 159 1e−15 62 4664 3027 700558314H1 SOYMON001 g2529376 BLASTX 149 1e−13 47 4665 3027 700786134H2 SOYMON011 g2529376 BLASTX 76 1e−12 57 4666 3027 700875943H1 SOYMON018 g2529376 BLASTX 107 1e−12 42 4667 3027 700741681H1 SOYMON012 g2529376 BLASTX 108 1e−10 46 4668 3027 701001530H1 SOYMON018 g14265 BLASTX 128 1e−10 83 4669 3027 701109215H1 SOYMON036 g2529375 BLASTN 257 1e−10 60 4670 3027 700891544H1 SOYMON024 g2529376 BLASTX 123 1e−9 44 4671 3027 LIB3054-002- LIB3054 g2529375 BLASTN 1026 1e−76 71 Q1-N1-B7 4672 3027 LIB3055-004- LIB3055 g2529375 BLASTN 423 1e−74 80 Q1-N1-B1 4673 3027 LIB3053-006- LIB3053 g2529375 BLASTN 973 1e−72 71 Q1-N1-B2 4674 3027 LIB3055-008- LIB3055 g2529375 BLASTN 684 1e−63 69 Q1-N1-H3 4675 3027 LIB3055-011- LIB3055 g2529375 BLASTN 483 1e−33 77 Q1-N1-F4 4676 3027 LIB3030-005- LIB3030 g2529375 BLASTN 315 1e−31 65 Q1-B1-E5 4677 3027 LIB3054-003- LIB3054 g2529375 BLASTN 256 1e−10 60 Q1-N1-E12 MAIZE D-RIBULOSE-5-PHOSPHATE-3-EPIMERASE 4678 -700222465 700222465H1 SATMON011 g1162980 BLASTX 149 1e−27 84 4679 -700618106 700618106H1 SATMON033 g902739 BLASTX 80 1e−25 76 4680 10201 700101610H1 SATMON009 g902738 BLASTN 1009 1e−75 80 4681 10201 700098237H1 SATMON009 g902738 BLASTN 1000 1e−74 80 4682 10201 700209605H1 SATMON016 g1162979 BLASTN 976 1e−72 78 4683 10201 700101988H1 SATMON009 g902738 BLASTN 626 1e−69 80 4684 10201 700091966H1 SATMON011 g902738 BLASTN 905 1e−66 80 4685 10201 700101445H1 SATMON009 g1162979 BLASTN 844 1e−61 80 4686 10201 700159349H1 SATMON012 g902738 BLASTN 681 1e−48 73 4687 10201 700380926H1 SATMON023 g902738 BLASTN 463 1e−45 81 4688 17215 700048475H1 SATMON003 g1008313 BLASTX 177 1e−17 61 4689 17215 700105805H1 SATMON010 g1008313 BLASTX 123 1e−10 59 4690 1795 700432796H1 SATMONN01 g902739 BLASTX 139 1e−12 93 4691 6043 700104089H1 SATMON010 g1162979 BLASTN 583 1e−39 79 4692 6043 700099362H1 SATMON009 g1162980 BLASTX 156 1e−29 71 4693 6043 700042321H1 SATMON004 g1162979 BLASTN 271 1e−27 79 4694 6043 700457795H1 SATMON029 g902739 BLASTX 132 1e−25 64 4695 6043 700096215H1 SATMON008 g1162980 BLASTX 120 1e−19 65 4696 6043 700378379H1 SATMON019 g1162980 BLASTX 119 1e−17 86 4697 6043 700239692H1 SATMON010 g1162980 BLASTX 167 1e−16 63 4698 6043 700093535H1 SATMON008 g1162980 BLASTX 120 1e−13 61 4699 6043 700098183H1 SATMON009 g1162980 BLASTX 121 1e−13 60 4700 6043 700093175H1 SATMON008 g902739 BLASTX 126 1e−12 59 4701 6043 700098056H1 SATMON009 g1162980 BLASTX 120 1e−9 57 4702 6043 700101650H1 SATMON009 g1162980 BLASTX 120 1e−9 57 4703 6043 700053356H1 SATMON009 g1162980 BLASTX 121 1e−9 57 4704 6043 700099441H1 SATMON009 g902739 BLASTX 122 1e−9 58 4705 7043 700162921H1 SATMON013 g1008313 BLASTX 130 1e−17 60 4706 7043 700552657H1 SATMON022 g902739 BLASTX 154 1e−16 51 4707 -L1891463 LIB189-001- LIB189 g1162979 BLASTN 596 1e−39 78 Q1-E1-F4 4708 -L30781313 LIB3078-002- LIB3078 g1162979 BLASTN 440 1e−25 79 Q1-K1-A2 4709 10201 LIB3078-034- LIB3078 g1162979 BLASTN 1271 1e−97 78 Q1-K1-E8 4710 10201 LIB189-018- LIB189 g902738 BLASTN 1263 1e−96 79 Q1-E1-G1 4711 10201 LIB3060-022- LIB3060 g902738 BLASTN 1228 1e−93 76 Q1-K1-G2 4712 10201 LIB3060-034- LIB3060 g902738 BLASTN 1205 1e−91 79 Q1-K1-D3 4713 10201 LIB36-007- LIB36 g1162979 BLASTN 989 1e−83 78 Q1-E1-D10 4714 10201 LIB3078-053- LIB3078 g1162979 BLASTN 850 1e−62 68 Q1-K1-F4 4715 10201 LIB189-034- LIB189 g902738 BLASTN 761 1e−53 74 Q1-E1-B12 4716 1795 LIB3067-056- LIB3067 g902738 BLASTN 645 1e−43 80 Q1-K1-A4 4717 6043 LIB189-017- LIB189 g1162979 BLASTN 842 1e−61 78 Q1-E1-F12 4718 6043 LIB36-012- LIB36 g1162979 BLASTN 742 1e−51 78 Q1-E1-H11 4719 6043 LIB3060-018- LIB3060 g1162979 BLASTN 653 1e−43 77 Q1-K1-B5 4720 6043 LIB3062-015- LIB3062 g1162979 BLASTN 637 1e−42 77 Q1-K1-A11 4721 6043 LIB189-031- LIB189 g1162979 BLASTN 532 1e−33 76 Q1-E1-D1 4722 6043 LIB3060-013- LIB3060 g1162979 BLASTN 466 1e−27 75 Q1-K1-A2 4723 7043 LIB148-032- LIB148 g2564973 BLASTX 238 1e−42 48 Q1-E1-A4 SOYBEAN D-RIBULOSE-5-PHOSPHATE-3-EPIMERASE 4724 -700677209 700677209H1 SOYMON007 g1162980 BLASTX 130 1e−30 85 4725 10469 700971857H1 SOYMON005 g1008313 BLASTX 208 1e−27 55 4726 10469 701064495H1 SOYMON034 g1008313 BLASTX 208 1e−27 56 4727 10469 701007767H1 SOYMON019 g1008313 BLASTX 129 1e−25 54 4728 10469 700656367H1 SOYMON004 g1008313 BLASTX 182 1e−22 57 4729 15209 700791582H1 SOYMON011 g2388956 BLASTX 129 1e−10 66 4730 15209 701001180H1 SOYMON018 g1008313 BLASTX 122 1e−9 65 4731 18337 700739263H1 SOYMON012 g902738 BLASTN 481 1e−50 82 4732 18337 700681545H1 SOYMON008 g1162979 BLASTN 342 1e−44 83 4733 18818 700866167H1 SOYMON016 g1162979 BLASTN 853 1e−62 89 4734 18818 700983968H1 SOYMON009 g1162979 BLASTN 422 1e−55 76 4735 5784 700999796H1 SOYMON018 g1162979 BLASTN 535 1e−43 78 4736 5784 700788240H1 SOYMON011 g902738 BLASTN 455 1e−36 77 4737 5784 701000905H1 SOYMON018 g902738 BLASTN 501 1e−36 77 4738 5784 701040171H1 SOYMON029 g902738 BLASTN 510 1e−33 78 4739 5784 700754807H1 SOYMON014 g902738 BLASTN 447 1e−31 72 4740 5784 700904930H1 SOYMON022 g902738 BLASTN 465 1e−29 77 4741 5784 700739828H1 SOYMON012 g902738 BLASTN 455 1e−28 76 4742 5784 700741008H1 SOYMON012 g1162980 BLASTX 142 1e−16 81 4743 5784 700738184H1 SOYMON012 g1162980 BLASTX 167 1e−16 81 4744 5784 700790753H1 SOYMON011 g1162980 BLASTX 149 1e−15 79 4745 5784 701110183H1 SOYMON036 g1162980 BLASTX 161 1e−15 81 4746 5784 700876264H1 SOYMON018 g1162980 BLASTX 140 1e−12 87 4747 5784 700787492H2 SOYMON011 g1162980 BLASTX 141 1e−12 76 4748 5784 700788242H1 SOYMON011 g1162980 BLASTX 80 1e−11 89 4749 5784 700741612H1 SOYMON012 g1162980 BLASTX 103 1e−11 78 4750 5784 700789926H2 SOYMON011 g1162980 BLASTX 119 1e−11 74 4751 5784 701105542H1 SOYMON036 g1162980 BLASTX 117 1e−10 66 4752 5784 700741161H1 SOYMON012 g1162980 BLASTX 101 1e−8 63 4753 5784 700877044H1 SOYMON018 g902738 BLASTN 236 1e−8 73 4754 9624 700659817H1 SOYMON004 g1162979 BLASTN 959 1e−71 85 4755 9624 700558457H1 SOYMON001 g1162979 BLASTN 533 1e−64 81 4756 9624 700898624H1 SOYMON027 g1162979 BLASTN 867 1e−63 83 4757 9624 700848716H1 SOYMON021 g1162979 BLASTN 680 1e−61 83 4758 9624 700990488H1 SOYMON011 g1162979 BLASTN 763 1e−54 83 4759 9624 700980873H1 SOYMON009 g1162979 BLASTN 722 1e−51 77 4760 9624 700654880H1 SOYMON004 g1162979 BLASTN 473 1e−36 71 4761 10469 LIB3040-057- LIB3040 g1008313 BLASTX 205 1e−60 54 Q1-E1-C5 4762 9624 LIB3030-001- LIB3030 g1162979 BLASTN 1185 1e−90 80 Q1-B1-F10 MAIZE RIBOSE-5-PHOSPHATE ISOMERASE 4763 5053 700206243H1 SATMON003 g1669358 BLASTX 165 1e−20 59 4764 5053 700157368H1 SATMON012 g1001678 BLASTX 188 1e−19 59 4765 -L30672312 LIB3067-007- LIB3067 g1789280 BLASTX 114 1e−24 54 Q1-K1-C3 4766 -L841459 LIB84-028- LIB84 g1789280 BLASTX 117 1e−25 53 Q1-E1-A11 4767 5053 LIB3078-033- LIB3078 g1001678 BLASTX 217 1e−42 50 Q1-K1-A2 4768 5053 LIB3060-054- LIB3060 g2649655 BLASTX 100 1e−34 48 Q1-K1-G1 4769 5053 LIB3078-054- LIB3078 g1669358 BLASTX 65 1e−24 40 Q1-K1-B9 MAIZE PUTATIVE RIBOSE-5-PHOSPHATE ISOMERASE 4770 -700622640 700622640H1 SATMON034 g3257798 BLASTX 128 1e−10 63 4771 5053 700213140H1 SATMON016 g500774 BLASTX 195 1e−20 43 SOYBEAN RIBOSE-5-PHOSPHATE ISOMERASE 4772 17047 700737894H1 SOYMON012 g1001678 BLASTX 93 1e−14 62 4773 17047 700790677H2 SOYMON011 g2649655 BLASTX 68 1e−9 47 4774 17047 700891079H1 SOYMON024 g1001678 BLASTX 122 1e−9 56 4775 8783 701120985H1 SOYMON037 g1789280 BLASTX 115 1e−9 51 4776 8783 700745725H1 SOYMON013 g1789280 BLASTX 113 1e−8 51 SOYBEAN PUTATIVE RIBOSE-5-PHOSPHATE ISOMERASE 4777 -700840778 700840778H1 SOYMON020 g500774 BLASTX 203 1e−21 51 4778 -700898355 700898355H1 SOYMON027 g3257798 BLASTX 108 1e−17 60 4779 16333 700562390H1 SOYMON002 g500774 BLASTX 211 1e−22 44 4780 16333 700961206H1 SOYMON022 g500774 BLASTX 145 1e−14 51 4781 8873 701120413H1 SOYMON037 g3257798 BLASTX 134 1e−11 48 MAIZE RIBOSE-5-PHOSPHATE KINASE 4782 -700427028 700427028H1 SATMONN01 g1885326 BLASTX 88 1e−11 60 4783 -700441954 700441954H1 SATMON026 g21840 BLASTN 186 1e−16 72 4784 -700448070 700448070H1 SATMON027 g16440 BLASTN 289 1e−39 75 4785 -700581778 700581778H1 SATMON031 g16441 BLASTX 117 1e−14 76 4786 3680 700044442H1 SATMON004 g21840 BLASTN 1134 1e−85 89 4787 3680 700044434H1 SATMON004 g21840 BLASTN 1122 1e−84 89 4788 3680 700430775H1 SATMONN01 g21840 BLASTN 1109 1e−83 87 4789 3680 700043261H1 SATMON004 g21840 BLASTN 1097 1e−82 90 4790 3680 700101266H1 SATMON009 g21840 BLASTN 1098 1e−82 88 4791 3680 700440552H1 SATMON026 g21840 BLASTN 1047 1e−78 89 4792 3680 700430385H1 SATMONN01 g21838 BLASTN 964 1e−71 88 4793 3680 700441643H1 SATMON026 g21840 BLASTN 852 1e−62 84 4794 3680 700042294H1 SATMON004 g21838 BLASTN 842 1e−61 86 4795 7956 700099212H1 SATMON009 g21840 BLASTN 1192 1e−90 86 4796 7956 700099715H1 SATMON009 g21840 BLASTN 1066 1e−80 85 4797 7956 700100470H1 SATMON009 g21840 BLASTN 925 1e−68 79 4798 7956 700438420H1 SATMON026 g21840 BLASTN 921 1e−67 84 4799 7956 700353611H1 SATMON024 g21838 BLASTN 812 1e−58 77 4800 7956 700100342H1 SATMON009 g21838 BLASTN 665 1e−46 76 4801 7956 700043758H1 SATMON004 g21840 BLASTN 394 1e−44 74 4802 7956 700100269H1 SATMON009 g21838 BLASTN 510 1e−32 73 4803 7956 700099313H1 SATMON009 g21838 BLASTN 516 1e−32 73 4804 7956 700097674H1 SATMON009 g21839 BLASTX 162 1e−30 76 4805 7956 700097907H1 SATMON009 g21840 BLASTN 455 1e−27 72 4806 7956 700098314H1 SATMON009 g21838 BLASTN 460 1e−27 72 4807 7956 700098714H1 SATMON009 g21840 BLASTN 462 1e−27 72 4808 7956 700101077H1 SATMON009 g21840 BLASTN 417 1e−24 69 4809 7956 700439560H1 SATMON026 g21838 BLASTN 421 1e−24 89 4810 7956 700094395H1 SATMON008 g21840 BLASTN 424 1e−24 70 4811 7956 700208768H1 SATMON016 g21840 BLASTN 424 1e−24 70 4812 7956 700100913H1 SATMON009 g21840 BLASTN 424 1e−24 70 4813 7956 700042685H1 SATMON004 g21840 BLASTN 401 1e−23 75 4814 7956 700097183H1 SATMON009 g21840 BLASTN 407 1e−23 75 4815 7956 700101216H1 SATMON009 g21839 BLASTX 97 1e−15 72 4816 -L361538 LIB36-008- LIB36 g21840 BLASTN 707 1e−48 82 Q1-E1-F4 4817 3680 LIB189-012- LIB189 g21840 BLASTN 1443 1e−130 86 Q1-E1-H11 4818 3680 LIB3078-011- LIB3078 g21840 BLASTN 1659 1e−129 88 Q1-K1-B10 4819 3680 LIB3066-004- LIB3066 g21840 BLASTN 1648 1e−128 87 Q1-K1-D6 4820 3680 LIB3060-025- LIB3060 g21840 BLASTN 1604 1e−127 88 Q1-K1-F6 4821 3680 LIB189-006- LIB189 g21840 BLASTN 1380 1e−106 89 Q1-E1-A5 4822 3680 LIB36-001- LIB36 g21840 BLASTN 1329 1e−101 78 Q1-E1-G1 4823 3680 LIB84-013- LIB84 g21840 BLASTN 919 1e−82 85 Q1-E1-B8 4824 3680 LIB36-014- LIB36 g21838 BLASTN 870 1e−70 86 Q1-E1-D8 4825 3680 LIB36-017- LIB36 g21838 BLASTN 589 1e−43 85 Q1-E1-H3 4826 7956 LIB189-029- LIB189 g21840 BLASTN 1559 1e−121 84 Q1-E1-D12 4827 7956 LIB3078-055- LIB3078 g21840 BLASTN 1370 1e−105 82 Q1-K1-D12 4828 7956 LIB36-020- LIB36 g21838 BLASTN 908 1e−93 76 Q1-E1-D1 4829 7956 LIB36-013- LIB36 g21838 BLASTN 792 1e−83 76 Q1-E1-B5 4830 7956 LIB3060-028- LIB3060 g21840 BLASTN 470 1e−73 76 Q1-K1-B7 4831 7956 LIB189-020- LIB189 g21840 BLASTN 411 1e−45 74 Q1-E1-B11 4832 7956 LIB3062-047- LIB3062 g21840 BLASTN 419 1e−28 71 Q1-K1-H1 SOYBEAN RIBOSE-5-PHOSPHATE KINASE 4833 -700657358 700657358H1 SOYMON004 g16441 BLASTX 134 1e−16 95 4834 -700790008 700790008H2 SOYMON011 g1885325 BLASTN 725 1e−51 75 4835 -700872439 700872439H1 SOYMON018 g1885325 BLASTN 562 1e−38 75 4836 4157 701055931H1 SOYMON032 g1885325 BLASTN 1147 1e−86 91 4837 4157 700680979H1 SOYMON008 g1885325 BLASTN 981 1e−84 85 4838 4157 700990472H1 SOYMON011 g1885325 BLASTN 1114 1e−84 88 4839 4157 700556547H1 SOYMON001 g1885325 BLASTN 1079 1e−81 87 4840 4157 700684029H1 SOYMON008 g1885325 BLASTN 1066 1e−80 87 4841 4157 700684302H1 SOYMON008 g1885325 BLASTN 1042 1e−78 89 4842 4157 700877162H1 SOYMON018 g1885325 BLASTN 922 1e−76 87 4843 4157 700875857H1 SOYMON018 g1885325 BLASTN 1021 1e−76 90 4844 4157 700875895H1 SOYMON018 g1885325 BLASTN 1027 1e−76 90 4845 4157 700791057H1 SOYMON011 g1885325 BLASTN 785 1e−75 89 4846 4157 700990257H1 SOYMON011 g1885325 BLASTN 1003 1e−74 86 4847 4157 700991766H1 SOYMON011 g1885325 BLASTN 622 1e−73 86 4848 4157 700875789H1 SOYMON018 g1885325 BLASTN 787 1e−71 90 4849 4157 700791651H1 SOYMON011 g1885325 BLASTN 949 1e−70 87 4850 4157 701106902H1 SOYMON036 g1885325 BLASTN 925 1e−68 85 4851 4157 700739192H1 SOYMON012 g1885325 BLASTN 916 1e−67 90 4852 4157 700681723H1 SOYMON008 g1885325 BLASTN 902 1e−66 85 4853 4157 700755385H1 SOYMON014 g1885325 BLASTN 883 1e−64 84 4854 4157 700870864H1 SOYMON018 g1885325 BLASTN 865 1e−63 78 4855 4157 701107593H1 SOYMON036 g1885325 BLASTN 872 1e−63 84 4856 4157 701002558H1 SOYMON018 g1885325 BLASTN 617 1e−62 84 4857 4157 700875430H1 SOYMON018 g1885325 BLASTN 860 1e−62 83 4858 4157 700654704H1 SOYMON004 g1885325 BLASTN 535 1e−58 86 4859 4157 701070469H1 SOYMON034 g1885325 BLASTN 214 1e−18 92 4860 4157 700739393H1 SOYMON012 g16441 BLASTX 182 1e−17 94 4861 4157 700657046H1 SOYMON004 g1885325 BLASTN 141 1e−10 86 4862 6097 700984236H1 SOYMON009 g1885325 BLASTN 1039 1e−77 87 4863 6097 701109839H1 SOYMON036 g1885325 BLASTN 952 1e−70 88 4864 6097 700731201H1 SOYMON009 g1885325 BLASTN 885 1e−64 85 4865 668 700959747H1 SOYMON022 g1885325 BLASTN 414 1e−65 84 4866 668 700994042H1 SOYMON011 g1885325 BLASTN 863 1e−63 82 4867 668 700899089H1 SOYMON027 g1885325 BLASTN 849 1e−61 84 4868 668 700787854H2 SOYMON011 g167265 BLASTN 330 1e−47 84 4869 668 700873392H1 SOYMON018 g167265 BLASTN 530 1e−35 85 4870 668 700553732H1 SOYMON001 g167265 BLASTN 483 1e−30 84 4871 668 700560501H1 SOYMON001 g167265 BLASTN 460 1e−27 84 4872 668 701105881H1 SOYMON036 g167265 BLASTN 439 1e−26 84 4873 668 700681112H2 SOYMON008 g167265 BLASTN 395 1e−22 85 4874 668 700997513H1 SOYMON018 g167265 BLASTN 383 1e−21 84 4875 668 700763831H1 SOYMON018 g167266 BLASTX 131 1e−16 84 4876 668 701055857H1 SOYMON032 g167266 BLASTX 163 1e−15 94 4877 668 700559450H1 SOYMON001 g167265 BLASTN 273 1e−15 78 4878 668 701000176H1 SOYMON018 g167266 BLASTX 155 1e−14 93 4879 668 700996108H1 SOYMON018 g167266 BLASTX 158 1e−14 84 4880 668 700791528H1 SOYMON011 g167265 BLASTN 298 1e−14 84 4881 668 700901050H1 SOYMON027 g167265 BLASTN 288 1e−13 83 4882 668 700979790H2 SOYMON009 g167265 BLASTN 288 1e−13 81 4883 668 700877128H1 SOYMON018 g167265 BLASTN 290 1e−13 74 4884 668 700743001H1 SOYMON012 g167266 BLASTX 140 1e−12 78 4885 668 700995911H1 SOYMON018 g167265 BLASTN 197 1e−12 86 4886 668 701106835H1 SOYMON036 g167265 BLASTN 278 1e−12 89 4887 668 700675621H1 SOYMON007 g167265 BLASTN 261 1e−11 75 4888 668 701002519H1 SOYMON018 g167266 BLASTX 125 1e−10 83 4889 668 700686660H1 SOYMON008 g167266 BLASTX 130 1e−10 83 4890 668 700738677H1 SOYMON012 g167265 BLASTN 196 1e−10 89 4891 668 700963637H1 SOYMON022 g167265 BLASTN 196 1e−10 88 4892 668 700791287H1 SOYMON011 g167265 BLASTN 236 1e−10 82 4893 668 700553943H1 SOYMON001 g167265 BLASTN 258 1e−10 83 4894 668 700876063H1 SOYMON018 g167266 BLASTX 116 1e−9 92 4895 668 700555924H1 SOYMON001 g167266 BLASTX 118 1e−9 79 4896 668 700686037H1 SOYMON008 g167265 BLASTN 249 1e−9 81 4897 668 700791185H1 SOYMON011 g167265 BLASTN 249 1e−9 86 4898 8098 700726396H1 SOYMON009 g1885325 BLASTN 711 1e−54 87 4899 8098 700683768H1 SOYMON008 g1885325 BLASTN 614 1e−45 87 4900 8098 700741625H1 SOYMON012 g1885325 BLASTN 479 1e−37 88 4901 8098 700737803H1 SOYMON012 g1885325 BLASTN 441 1e−29 86 4902 8098 700995703H1 SOYMON011 g1885325 BLASTN 286 1e−14 85 4903 4157 LIB3055-013- LIB3055 g1885325 BLASTN 1123 1e−131 87 Q1-N1-F6 4904 4157 LIB3028-012- LIB3028 g1885325 BLASTN 645 1e−82 81 Q1-B1-F10 4905 668 LIB3039-054- LIB3039 g167265 BLASTN 815 1e−64 80 Q1-E1-C11 4906 668 LIB3055-013- LIB3055 g167265 BLASTN 817 1e−59 83 Q1-N1-D11 4907 668 LIB3055-013- LIB3055 g167265 BLASTN 676 1e−45 79 Q1-N1-H7 4908 668 LIB3055-004- LIB3055 g1885325 BLASTN 318 1e−36 83 Q1-N1-F5 MAIZE PHOSPHOENOLPYRUVATE CARBOXYLASE 4909 -700029657 700029657H1 SATMON003 g22614 BLASTN 275 1e−13 83 4910 -700043027 700043027H1 SATMON004 g22407 BLASTN 497 1e−38 80 4911 -700073205 700073205H1 SATMON007 g3132309 BLASTN 1480 1e−114 100 4912 -700073954 700073954H1 SATMON007 g22614 BLASTN 243 1e−28 79 4913 -700075634 700075634H1 SATMON007 g3132309 BLASTN 471 1e−75 83 4914 -700076492 700076492H1 SATMON007 g429148 BLASTN 909 1e−109 98 4915 -700097250 700097250H1 SATMON009 g22396 BLASTN 366 1e−21 88 4916 -700100473 700100473H1 SATMON009 g22407 BLASTN 644 1e−63 98 4917 -700101359 700101359H1 SATMON009 g22415 BLASTN 1530 1e−118 99 4918 -700152625 700152625H1 SATMON007 g3132309 BLASTN 1154 1e−87 99 4919 -700154435 700154435H1 SATMON007 g3132309 BLASTN 761 1e−54 98 4920 -700162895 700162895H1 SATMON013 g169843 BLASTN 438 1e−27 85 4921 -700201740 700201740H1 SATMON003 g21629 BLASTN 498 1e−32 86 4922 -700224677 700224677H1 SATMON011 g429148 BLASTN 729 1e−84 95 4923 -700238706 700238706H1 SATMON010 g429148 BLASTN 1431 1e−110 99 4924 -700257537 700257537H1 SATMON017 g22409 BLASTN 391 1e−50 91 4925 -700331923 700331923H1 SATMON019 g429148 BLASTN 1338 1e−102 97 4926 -700356223 700356223H1 SATMON024 g21629 BLASTN 471 1e−79 96 4927 -700356594 700356594H1 SATMON024 g21629 BLASTN 117 1e−8 95 4928 -700428887 700428887H1 SATMONN01 g22407 BLASTN 303 1e−31 85 4929 -700429388 700429388H1 SATMONN01 g22468 BLASTN 221 1e−22 89 4930 -700441559 700441559H1 SATMON026 g22396 BLASTN 194 1e−10 90 4931 -700552009 700552009H1 SATMON022 g169843 BLASTN 739 1e−84 94 4932 -700578607 700578607H1 SATMON031 g22390 BLASTN 380 1e−35 99 4933 -701169553 701169553H1 SATMONN05 g18463 BLASTN 271 1e−13 66 4934 10799 700074427H1 SATMON007 g3132309 BLASTN 1458 1e−112 99 4935 10799 700154441H1 SATMON007 g3132309 BLASTN 1090 1e−81 100 4936 1418 700097963H1 SATMON009 g22396 BLASTN 1635 1e−127 100 4937 1418 700097754H1 SATMON009 g22415 BLASTN 1080 1e−124 100 4938 1418 700097792H1 SATMON009 g22407 BLASTN 1598 1e−124 99 4939 1418 700098551H1 SATMON009 g22407 BLASTN 1296 1e−123 97 4940 1418 700098302H1 SATMON009 g22415 BLASTN 1588 1e−123 99 4941 1418 700098121H1 SATMON009 g22415 BLASTN 1582 1e−122 99 4942 1418 700101619H1 SATMON009 g22396 BLASTN 1561 1e−121 99 4943 1418 700098581H1 SATMON009 g22415 BLASTN 1571 1e−121 98 4944 1418 700099632H1 SATMON009 g22407 BLASTN 1556 1e−120 99 4945 1418 700101969H1 SATMON009 g22562 BLASTN 1539 1e−119 99 4946 1418 700083104H1 SATMON011 g22415 BLASTN 1082 1e−118 97 4947 1418 700100275H1 SATMON009 g22407 BLASTN 1534 1e−118 99 4948 1418 700098816H1 SATMON009 g22562 BLASTN 926 1e−117 98 4949 1418 700101994H1 SATMON009 g22415 BLASTN 1512 1e−117 99 4950 1418 700101641H1 SATMON009 g22396 BLASTN 1515 1e−117 100 4951 1418 700101001H1 SATMON009 g22415 BLASTN 1500 1e−116 100 4952 1418 700099730H1 SATMON009 g22396 BLASTN 1500 1e−116 100 4953 1418 700097140H1 SATMON009 g22562 BLASTN 1506 1e−116 99 4954 1418 700100324H1 SATMON009 g22415 BLASTN 1260 1e−115 100 4955 1418 700098727H1 SATMON009 g22415 BLASTN 1487 1e−115 99 4956 1418 700097485H1 SATMON009 g22415 BLASTN 1496 1e−115 99 4957 1418 700097789H1 SATMON009 g22407 BLASTN 1479 1e−114 99 4958 1418 700099540H1 SATMON009 g22415 BLASTN 1485 1e−114 100 4959 1418 700097905H1 SATMON009 g22415 BLASTN 1224 1e−113 98 4960 1418 700099338H1 SATMON009 g22407 BLASTN 1248 1e−113 99 4961 1418 700101618H1 SATMON009 g22415 BLASTN 1395 1e−113 100 4962 1418 700100382H1 SATMON009 g22415 BLASTN 1465 1e−113 100 4963 1418 700097861H1 SATMON009 g22396 BLASTN 1473 1e−113 99 4964 1418 700099369H1 SATMON009 g22415 BLASTN 1457 1e−112 99 4965 1418 700097270H1 SATMON009 g22407 BLASTN 1383 1e−111 97 4966 1418 700042158H1 SATMON004 g22415 BLASTN 1440 1e−111 100 4967 1418 700097169H1 SATMON009 g22415 BLASTN 1427 1e−110 97 4968 1418 700099238H1 SATMON009 g22415 BLASTN 1428 1e−110 99 4969 1418 700045908H1 SATMON004 g22415 BLASTN 1424 1e−109 97 4970 1418 700101654H1 SATMON009 g22415 BLASTN 985 1e−108 99 4971 1418 700041622H1 SATMON004 g22415 BLASTN 1403 1e−108 99 4972 1418 700099014H1 SATMON009 g22415 BLASTN 1403 1e−108 99 4973 1418 700045755H1 SATMON004 g22415 BLASTN 1405 1e−108 100 4974 1418 700097929H1 SATMON009 g22415 BLASTN 1405 1e−108 95 4975 1418 700101507H1 SATMON009 g22415 BLASTN 927 1e−107 98 4976 1418 700101139H1 SATMON009 g22415 BLASTN 1394 1e−107 97 4977 1418 700042011H1 SATMON004 g22415 BLASTN 1395 1e−107 100 4978 1418 700099449H1 SATMON009 g22415 BLASTN 1399 1e−107 98 4979 1418 700097495H1 SATMON009 g22407 BLASTN 1028 1e−106 99 4980 1418 700404862H1 SATMON026 g22415 BLASTN 1276 1e−106 99 4981 1418 700041640H1 SATMON004 g22562 BLASTN 1385 1e−106 100 4982 1418 700042815H1 SATMON004 g22396 BLASTN 1385 1e−106 100 4983 1418 700099760H1 SATMON009 g22415 BLASTN 751 1e−105 97 4984 1418 700098974H1 SATMON009 g22407 BLASTN 900 1e−105 97 4985 1418 700046051H1 SATMON004 g22396 BLASTN 1341 1e−105 99 4986 1418 700098022H1 SATMON009 g22415 BLASTN 1367 1e−105 99 4987 1418 700044753H1 SATMON004 g22407 BLASTN 1370 1e−105 100 4988 1418 700044255H1 SATMON004 g22415 BLASTN 1370 1e−105 100 4989 1418 700043411H1 SATMON004 g22396 BLASTN 1375 1e−105 100 4990 1418 700046087H1 SATMON004 g22415 BLASTN 1375 1e−105 100 4991 1418 700041663H1 SATMON004 g22407 BLASTN 1378 1e−105 99 4992 1418 700099451H1 SATMON009 g22415 BLASTN 1301 1e−104 95 4993 1418 700043646H1 SATMON004 g22407 BLASTN 1350 1e−103 100 4994 1418 700045303H1 SATMON004 g22415 BLASTN 1350 1e−103 100 4995 1418 700223981H1 SATMON011 g22407 BLASTN 1352 1e−103 99 4996 1418 700043601H1 SATMON004 g22396 BLASTN 1115 1e−102 100 4997 1418 700043020H1 SATMON004 g22415 BLASTN 1331 1e−102 99 4998 1418 700046435H1 SATMON004 g22415 BLASTN 1335 1e−102 100 4999 1418 700100821H1 SATMON009 g22415 BLASTN 1340 1e−102 100 5000 1418 700044311H1 SATMON004 g22396 BLASTN 1290 1e−101 100 5001 1418 700042492H1 SATMON004 g22415 BLASTN 1325 1e−101 100 5002 1418 700045679H1 SATMON004 g22562 BLASTN 1326 1e−101 99 5003 1418 700043854H1 SATMON004 g22396 BLASTN 1328 1e−101 99 5004 1418 700097174H1 SATMON009 g22407 BLASTN 579 1e−100 97 5005 1418 700043617H1 SATMON004 g22415 BLASTN 1172 1e−100 98 5006 1418 700043213H1 SATMON004 g22415 BLASTN 1307 1e−100 99 5007 1418 700044283H1 SATMON004 g22562 BLASTN 1315 1e−100 100 5008 1418 700044758H1 SATMON004 g22562 BLASTN 1317 1e−100 99 5009 1418 700045971H1 SATMON004 g22415 BLASTN 1318 1e−100 99 5010 1418 700045753H1 SATMON004 g22415 BLASTN 1268 1e−99 95 5011 1418 700044982H1 SATMON004 g22415 BLASTN 1300 1e−99 100 5012 1418 700045990H1 SATMON004 g22415 BLASTN 1303 1e−99 99 5013 1418 700222578H1 SATMON011 g22415 BLASTN 1286 1e−98 97 5014 1418 700101090H1 SATMON009 g22396 BLASTN 1152 1e−97 99 5015 1418 700044587H1 SATMON004 g22396 BLASTN 1279 1e−97 99 5016 1418 700100745H1 SATMON009 g22396 BLASTN 1280 1e−97 100 5017 1418 700043547H1 SATMON004 g22562 BLASTN 1281 1e−97 95 5018 1418 700428356H1 SATMONN01 g22407 BLASTN 1035 1e−96 98 5019 1418 700219747H1 SATMON011 g22562 BLASTN 1261 1e−96 99 5020 1418 700045081H1 SATMON004 g22396 BLASTN 1263 1e−96 99 5021 1418 700101816H1 SATMON009 g22396 BLASTN 1250 1e−95 100 5022 1418 700042889H1 SATMON004 g22562 BLASTN 722 1e−94 98 5023 1418 700041694H1 SATMON004 g22415 BLASTN 831 1e−94 98 5024 1418 700098977H1 SATMON009 g22562 BLASTN 933 1e−94 97 5025 1418 700423950H1 SATMONN01 g22396 BLASTN 1187 1e−94 99 5026 1418 700053467H1 SATMON009 g22415 BLASTN 821 1e−92 93 5027 1418 700042228H1 SATMON004 g22415 BLASTN 841 1e−91 98 5028 1418 700044924H1 SATMON004 g22396 BLASTN 1205 1e−91 100 5029 1418 700438595H1 SATMON026 g22407 BLASTN 620 1e−90 99 5030 1418 700422253H1 SATMONN01 g22396 BLASTN 781 1e−89 95 5031 1418 700044946H1 SATMON004 g22396 BLASTN 1170 1e−88 100 5032 1418 700025647H1 SATMON004 g22407 BLASTN 1128 1e−87 98 5033 1418 700213665H1 SATMON016 g22415 BLASTN 1161 1e−87 99 5034 1418 700100741H1 SATMON009 g22407 BLASTN 1137 1e−85 95 5035 1418 700045039H1 SATMON004 g22562 BLASTN 722 1e−84 99 5036 1418 700042588H1 SATMON004 g22396 BLASTN 1119 1e−84 99 5037 1418 700209485H1 SATMON016 g22415 BLASTN 771 1e−82 95 5038 1418 700198048H1 SATMON016 g22407 BLASTN 812 1e−80 97 5039 1418 700424537H1 SATMONN01 g22396 BLASTN 1070 1e−80 87 5040 1418 700439340H1 SATMON026 g22415 BLASTN 725 1e−76 97 5041 1418 700439420H1 SATMON026 g22415 BLASTN 1017 1e−75 94 5042 1418 700098640H1 SATMON009 g22562 BLASTN 991 1e−73 99 5043 1418 700427059H1 SATMONN01 g22396 BLASTN 523 1e−69 92 5044 1418 700099478H1 SATMON009 g22415 BLASTN 721 1e−69 100 5045 1418 700425005H1 SATMONN01 g22415 BLASTN 939 1e−69 97 5046 1418 700101925H1 SATMON009 g22562 BLASTN 878 1e−64 99 5047 1418 700099430H1 SATMON009 g22415 BLASTN 824 1e−59 98 5048 1418 700429358H1 SATMONN01 g22407 BLASTN 548 1e−57 98 5049 1418 700447220H1 SATMON027 g22562 BLASTN 799 1e−57 98 5050 1418 700100706H1 SATMON009 g22407 BLASTN 770 1e−55 100 5051 1418 700209112H1 SATMON016 g22415 BLASTN 593 1e−54 98 5052 1418 700098367H1 SATMON009 g22415 BLASTN 698 1e−49 99 5053 1418 700045489H1 SATMON004 g22407 BLASTN 642 1e−44 92 5054 1418 700043353H1 SATMON004 g22396 BLASTN 645 1e−44 100 5055 1418 700097654H1 SATMON009 g22407 BLASTN 618 1e−42 99 5056 1418 700423550H1 SATMONN01 g22396 BLASTN 599 1e−41 88 5057 1418 700439981H1 SATMON026 g22407 BLASTN 590 1e−40 96 5058 1418 700097894H1 SATMON009 g22407 BLASTN 570 1e−38 100 5059 1418 700423563H1 SATMONN01 g22407 BLASTN 516 1e−34 99 5060 1418 700213765H1 SATMON016 g22407 BLASTN 484 1e−31 97 5061 1418 700043914H1 SATMON004 g22407 BLASTN 261 1e−26 93 5062 1418 700434554H1 SATMONN01 g22396 BLASTN 397 1e−24 87 5063 1418 700088748H1 SATMON011 g22396 BLASTN 292 1e−15 89 5064 1418 700097692H1 SATMON009 g22396 BLASTN 255 1e−13 98 5065 16592 700098887H1 SATMON009 g22415 BLASTN 1526 1e−118 99 5066 16592 700101171H1 SATMON009 g22415 BLASTN 1481 1e−114 99 5067 16592 700098335H1 SATMON009 g22415 BLASTN 1455 1e−112 100 5068 16592 700101419H1 SATMON009 g22415 BLASTN 1450 1e−111 100 5069 16592 700098187H1 SATMON009 g22562 BLASTN 877 1e−110 98 5070 16592 700099874H1 SATMON009 g22562 BLASTN 1427 1e−109 97 5071 16592 700098983H1 SATMON009 g22415 BLASTN 1355 1e−104 98 5072 16592 700045302H1 SATMON004 g22412 BLASTN 704 1e−99 96 5073 16592 700218247H1 SATMON016 g22412 BLASTN 710 1e−99 98 5074 16592 700100826H1 SATMON009 g22412 BLASTN 710 1e−98 97 5075 16592 700098774H1 SATMON009 g22562 BLASTN 1190 1e−97 93 5076 16592 700101312H1 SATMON009 g22562 BLASTN 1210 1e−96 91 5077 16592 700053403H1 SATMON009 g22415 BLASTN 1260 1e−96 94 5078 16592 700045034H1 SATMON004 g22562 BLASTN 1189 1e−90 99 5079 16592 700097293H1 SATMON009 g22412 BLASTN 667 1e−86 92 5080 17901 700578474H1 SATMON031 g22415 BLASTN 979 1e−72 98 5081 17901 700578374H1 SATMON031 g22415 BLASTN 491 1e−63 98 5082 1943 700549932H1 SATMON022 g429148 BLASTN 914 1e−67 80 5083 1943 700020030H1 SATMON001 g429148 BLASTN 686 1e−48 79 5084 19736 700264360H1 SATMON017 g429148 BLASTN 1519 1e−117 98 5085 19736 700238856H1 SATMON010 g429148 BLASTN 754 1e−102 99 5086 201 700074903H1 SATMON007 g3132309 BLASTN 820 1e−119 100 5087 201 700620292H1 SATMON034 g3132309 BLASTN 940 1e−113 100 5088 201 700616392H1 SATMON033 g3132309 BLASTN 1008 1e−107 99 5089 201 700049716H1 SATMON003 g3132309 BLASTN 1018 1e−107 99 5090 201 700028563H1 SATMON003 g3132309 BLASTN 1361 1e−104 99 5091 201 700105527H1 SATMON010 g3132309 BLASTN 1319 1e−100 99 5092 201 700615230H1 SATMON033 g3132309 BLASTN 955 1e−99 99 5093 201 700550579H1 SATMON022 g3132309 BLASTN 737 1e−98 99 5094 201 700381592H1 SATMON023 g3132309 BLASTN 974 1e−97 92 5095 201 701186231H1 SATMONN06 g3132309 BLASTN 918 1e−96 97 5096 201 700572736H1 SATMON030 g3132309 BLASTN 963 1e−96 96 5097 201 700158658H1 SATMON012 g3132309 BLASTN 936 1e−93 99 5098 201 701186212H1 SATMONN06 g3132309 BLASTN 971 1e−92 98 5099 201 700616621H1 SATMON033 g3132309 BLASTN 780 1e−87 92 5100 201 701161255H1 SATMONN04 g3132309 BLASTN 856 1e−87 98 5101 201 700222259H1 SATMON011 g3132309 BLASTN 1148 1e−86 92 5102 201 701161671H1 SATMONN04 g3132309 BLASTN 886 1e−81 98 5103 201 700028609H1 SATMON003 g21629 BLASTN 525 1e−75 92 5104 201 700570011H1 SATMON030 g3132309 BLASTN 696 1e−75 98 5105 201 700467579H1 SATMON025 g3132309 BLASTN 901 1e−70 96 5106 201 700020751H1 SATMON001 g3132309 BLASTN 489 1e−44 89 5107 201 700612494H1 SATMON033 g3132309 BLASTN 341 1e−28 97 5108 20363 700028168H1 SATMON003 g429148 BLASTN 891 1e−109 98 5109 20363 700150081H1 SATMON007 g429148 BLASTN 660 1e−75 99 5110 21797 700104081H1 SATMON010 g22468 BLASTN 1240 1e−96 100 5111 21797 700258244H1 SATMON017 g3132309 BLASTN 1115 1e−84 100 5112 21797 700206542H1 SATMON003 g22468 BLASTN 1000 1e−76 100 5113 22719 700238111H1 SATMON010 g3132309 BLASTN 1286 1e−105 98 5114 22719 700804782H1 SATMON036 g3132309 BLASTN 725 1e−90 100 5115 23787 700050530H1 SATMON003 g169843 BLASTN 1266 1e−96 92 5116 23787 701180159H1 SATMONN05 g169843 BLASTN 1108 1e−83 92 5117 2554 700160214H1 SATMON012 g429148 BLASTN 1310 1e−100 100 5118 2554 700553034H1 SATMON022 g429148 BLASTN 1111 1e−83 99 5119 2554 700168584H1 SATMON013 g429148 BLASTN 1075 1e−80 100 5120 2594 700257383H1 SATMON017 g3132309 BLASTN 469 1e−51 91 5121 2594 700263133H1 SATMON017 g3132309 BLASTN 545 1e−42 97 5122 2724 700213133H1 SATMON016 g429148 BLASTN 1190 1e−106 98 5123 2724 700087946H1 SATMON011 g429148 BLASTN 1103 1e−83 99 5124 30586 700170629H1 SATMON013 g169843 BLASTN 880 1e−64 88 5125 3591 700451602H1 SATMON028 g429148 BLASTN 730 1e−102 99 5126 3591 700243536H1 SATMON010 g429148 BLASTN 926 1e−90 99 5127 3591 700104327H1 SATMON010 g429148 BLASTN 1038 1e−77 97 5128 3591 701160410H1 SATMONN04 g429148 BLASTN 568 1e−65 85 5129 4329 700051281H1 SATMON003 g3132309 BLASTN 1520 1e−117 100 5130 4329 700075340H1 SATMON007 g3132309 BLASTN 1490 1e−115 100 5131 4329 700259374H1 SATMON017 g3132309 BLASTN 1451 1e−111 99 5132 4329 700026464H1 SATMON003 g3132309 BLASTN 1405 1e−108 100 5133 4329 700075594H1 SATMON007 g3132309 BLASTN 1395 1e−107 100 5134 4329 700074584H1 SATMON007 g3132309 BLASTN 1397 1e−107 97 5135 4329 700211639H1 SATMON016 g3132309 BLASTN 1310 1e−100 95 5136 4329 700477352H1 SATMON025 g3132309 BLASTN 685 1e−98 99 5137 4329 700212885H1 SATMON016 g3132309 BLASTN 1262 1e−96 97 5138 4329 700150132H1 SATMON007 g3132309 BLASTN 1193 1e−90 99 5139 4329 700150124H1 SATMON007 g3132309 BLASTN 1175 1e−89 100 5140 4329 700382807H1 SATMON024 g3132309 BLASTN 785 1e−87 98 5141 4329 700219884H1 SATMON011 g3132309 BLASTN 905 1e−81 98 5142 4329 700203986H1 SATMON003 g3132309 BLASTN 1078 1e−80 99 5143 4329 700155306H1 SATMON007 g21629 BLASTN 838 1e−60 92 5144 4329 700474781H1 SATMON025 g3132309 BLASTN 353 1e−39 94 5145 4530 700574802H1 SATMON030 g429148 BLASTN 1236 1e−113 98 5146 4530 700049340H1 SATMON003 g429148 BLASTN 1185 1e−110 100 5147 4530 701180032H1 SATMONN05 g429148 BLASTN 954 1e−95 99 5148 4530 700611642H1 SATMON022 g429148 BLASTN 1059 1e−84 94 5149 4530 700203138H1 SATMON003 g429148 BLASTN 883 1e−71 96 5150 4530 700029976H1 SATMON003 g429148 BLASTN 805 1e−68 97 5151 7486 700614328H1 SATMON033 g169843 BLASTN 1437 1e−110 96 5152 7486 700352909H1 SATMON024 g169843 BLASTN 1035 1e−77 96 5153 8267 700073585H1 SATMON007 g429148 BLASTN 1395 1e−107 100 5154 8267 700023118H1 SATMON003 g429148 BLASTN 1266 1e−96 99 5155 8267 700456524H1 SATMON029 g429148 BLASTN 743 1e−92 95 5156 8267 700030070H1 SATMON003 g429148 BLASTN 890 1e−70 95 5157 8340 700077313H1 SATMON007 g3132309 BLASTN 1575 1e−122 100 5158 8340 700381893H1 SATMON023 g21629 BLASTN 1329 1e−101 96 5159 8340 700574357H2 SATMON030 g3132309 BLASTN 1040 1e−100 100 5160 8340 700548421H1 SATMON022 g3132309 BLASTN 1217 1e−99 94 5161 8340 700029043H1 SATMON003 g3132309 BLASTN 1273 1e−97 99 5162 8340 700553323H1 SATMON022 g3132309 BLASTN 1276 1e−97 99 5163 8340 700167824H1 SATMON013 g3132309 BLASTN 1190 1e−90 100 5164 8340 700153945H1 SATMON007 g3132309 BLASTN 1113 1e−83 99 5165 8340 700615517H1 SATMON033 g3132309 BLASTN 874 1e−76 96 5166 8340 700265822H1 SATMON017 g3132309 BLASTN 755 1e−54 100 5167 9226 700223020H1 SATMON011 g169843 BLASTN 1098 1e−82 92 5168 9226 700613182H1 SATMON033 g169843 BLASTN 936 1e−76 91 5169 -L1437153 LIB143-036- LIB143 g18463 BLASTN 262 1e−12 66 Q1-E1-D6 5170 -L1482958 LIB148-011- LIB148 g18463 BLASTN 211 1e−8 72 Q1-E1-D6 5171 -L1893647 LIB189-031- LIB189 g22407 BLASTN 888 1e−76 81 Q1-E1-H12 5172 -L30596200 LIB3059-060- LIB3059 g169843 BLASTN 276 1e−11 76 Q1-K1-G6 5173 -L30602129 LIB3060-009- LIB3060 g22415 BLASTN 369 1e−70 91 Q1-K1-C3 5174 -L30602452 LIB3060-011- LIB3060 g22396 BLASTN 198 1e−15 82 Q1-K1-F9 5175 -L30603203 LIB3060-029- LIB3060 g22407 BLASTN 1486 1e−114 83 Q1-K1-A8 5176 -L30604116 LIB3060-040- LIB3060 g18463 BLASTN 260 1e−12 64 Q1-K1-D7 5177 -L30604857 LIB3060-020- LIB3060 g22407 BLASTN 459 1e−40 86 Q1-K1-G9 5178 -L30606181 LIB3060-019- LIB3060 g22407 BLASTN 254 1e−38 69 Q1-K1-B5 5179 -L30684867 LIB3068-040- LIB3068 g18463 BLASTN 216 1e−9 69 Q1-K1-A3 5180 -L30684926 LIB3068-040- LIB3068 g18463 BLASTN 264 1e−11 64 Q1-K1-H6 5181 -L30686577 LIB3068-010- LIB3068 g18463 BLASTN 209 1e−8 71 Q1-K1-E2 5182 -L30695246 LIB3069-036- LIB3069 g169843 BLASTN 257 1e−10 79 Q1-K1-G3 5183 -L30695363 LIB3069-035- LIB3069 g429148 BLASTN 371 1e−35 91 Q1-K1-D7 5184 -L30782259 LIB3078-007- LIB3078 g22415 BLASTN 548 1e−46 72 Q1-K1-E3 5185 -L30783285 LIB3078-051- LIB3078 g22415 BLASTN 941 1e−84 78 Q1-K1-F1 5186 -L361508 LIB36-008- LIB36 g22415 BLASTN 825 1e−59 90 Q1-E1-B4 5187 -L362677 LIB36-007- LIB36 g22614 BLASTN 235 1e−8 77 Q1-E1-G11 5188 -L841179 LIB84-013- LIB84 g22415 BLASTN 594 1e−40 81 Q1-E1-A10 5189 -L841868 LIB84-029- LIB84 g18463 BLASTN 237 1e−10 66 Q1-E1-F12 5190 1418 LIB36-002- LIB36 g22562 BLASTN 2116 1e−177 99 Q1-E1-G4 5191 1418 LIB36-002- LIB36 g22562 BLASTN 2184 1e−173 98 Q1-E1-E9 5192 1418 LIB36-002- LIB36 g22415 BLASTN 2175 1e−172 98 Q1-E1-D11 5193 1418 LIB3060-035- LIB3060 g22415 BLASTN 2143 1e−169 98 Q1-K1-E11 5194 1418 LIB3060-003- LIB3060 g22407 BLASTN 2003 1e−168 98 Q1-K1-E12 5195 1418 LIB3060-012- LIB3060 g22407 BLASTN 2127 1e−168 98 Q1-K1-F9 5196 1418 LIB36-009- LIB36 g22396 BLASTN 2133 1e−168 99 Q1-E1-D9 5197 1418 LIB3078-014- LIB3078 g22415 BLASTN 2117 1e−167 99 Q1-K1-G9 5198 1418 LIB36-003- LIB36 g22396 BLASTN 2107 1e−166 98 Q1-E1-G4 5199 1418 LIB3060-016- LIB3060 g22407 BLASTN 2096 1e−165 99 Q1-K1-A6 5200 1418 LIB3060-021- LIB3060 g22415 BLASTN 1532 1e−164 97 Q1-K1-E1 5201 1418 LIB36-013- LIB36 g22415 BLASTN 2067 1e−163 98 Q1-E1-A10 5202 1418 LIB36-012- LIB36 g22415 BLASTN 1865 1e−161 97 Q1-E1-E3 5203 1418 LIB36-003- LIB36 g22415 BLASTN 2048 1e−161 97 Q1-E1-B9 5204 1418 LIB3078-015- LIB3078 g22396 BLASTN 2005 1e−158 99 Q1-K1-F11 5205 1418 LIB189-024- LIB189 g22396 BLASTN 2007 1e−158 99 Q1-E1-A11 5206 1418 LIB36-002- LIB36 g22415 BLASTN 2013 1e−158 92 Q1-E1-C1 5207 1418 LIB3078-056- LIB3078 g22562 BLASTN 1612 1e−157 90 Q1-K1-B2 5208 1418 LIB3060-048- LIB3060 g22415 BLASTN 1824 1e−156 92 Q1-K1-A9 5209 1418 LIB189-011- LIB189 g22415 BLASTN 1849 1e−156 96 Q1-E1-F6 5210 1418 LIB3060-054- LIB3060 g22415 BLASTN 1912 1e−156 96 Q1-K1-E7 5211 1418 LIB3078-016- LIB3078 g22562 BLASTN 1960 1e−156 99 Q1-K1-C2 5212 1418 LIB3060-009- LIB3060 g22562 BLASTN 1626 1e−155 94 Q1-K1-C11 5213 1418 LIB36-003- LIB36 g22562 BLASTN 1841 1e−154 97 Q1-E1-F7 5214 1418 LIB3060-045- LIB3060 g22407 BLASTN 1353 1e−153 95 Q1-K1-B2 5215 1418 LIB3060-052- LIB3060 g22407 BLASTN 1041 1e−152 95 Q1-K1-B6 5216 1418 LIB36-018- LIB36 g22415 BLASTN 1637 1e−152 92 Q1-E1-D4 5217 1418 LIB189-024- LIB189 g22396 BLASTN 1939 1e−152 93 Q1-E1-E3 5218 1418 LIB36-010- LIB36 g22396 BLASTN 1004 1e−151 94 Q1-E1-H4 5219 1418 LIB3060-012- LIB3060 g22415 BLASTN 1532 1e−150 90 Q1-K1-B10 5220 1418 LIB3060-019- LIB3060 g22415 BLASTN 1919 1e−150 97 Q1-K1-G7 5221 1418 LIB36-022- LIB36 g22562 BLASTN 1851 1e−149 95 Q1-E1-E7 5222 1418 LIB3060-021- LIB3060 g22562 BLASTN 869 1e−147 94 Q1-K1-C2 5223 1418 LIB3060-053- LIB3060 g22415 BLASTN 1578 1e−145 93 Q1-K1-D6 5224 1418 LIB189-006- LIB189 g22415 BLASTN 1682 1e−145 99 Q1-E1-D4 5225 1418 LIB3060-011- LIB3060 g22415 BLASTN 1712 1e−144 96 Q1-K1-A5 5226 1418 LIB189-022- LIB189 g22562 BLASTN 1774 1e−144 96 Q1-E1-H8 5227 1418 LIB3061-017- LIB3061 g22562 BLASTN 1533 1e−142 93 Q1-K1-E11 5228 1418 LIB83-002- LIB83 g22415 BLASTN 1122 1e−140 95 Q1-E1-E1 5229 1418 LIB3060-020- LIB3060 g22415 BLASTN 1542 1e−139 93 Q1-K1-C10 5230 1418 LIB3060-041- LIB3060 g22407 BLASTN 1602 1e−136 98 Q1-K1-G7 5231 1418 LIB189-016- LIB189 g22562 BLASTN 1318 1e−135 95 Q1-E1-C1 5232 1418 LIB189-031- LIB189 g22415 BLASTN 1613 1e−134 95 Q1-E1-H11 5233 1418 LIB189-028- LIB189 g22562 BLASTN 1600 1e−130 100 Q1-E1-B6 5234 1418 LIB36-019- LIB36 g22415 BLASTN 1245 1e−129 96 Q1-E1-A5 5235 1418 LIB3060-023- LIB3060 g22415 BLASTN 1650 1e−128 81 Q1-K1-G11 5236 1418 LIB36-018- LIB36 g22396 BLASTN 1228 1e−127 96 Q1-E1-A4 5237 1418 LIB3060-008- LIB3060 g22396 BLASTN 1570 1e−126 99 Q1-K1-B10 5238 1418 LIB83-009- LIB83 g22562 BLASTN 1421 1e−123 98 Q1-E1-A11 5239 1418 LIB189-002- LIB189 g22562 BLASTN 1477 1e−122 99 Q1-E1-B7 5240 1418 LIB3060-045- LIB3060 g22562 BLASTN 1078 1e−121 90 Q1-K1-B1 5241 1418 LIB36-007- LIB36 g22415 BLASTN 1536 1e−119 98 Q1-E1-A11 5242 1418 LIB36-006- LIB36 g22407 BLASTN 1304 1e−117 97 Q1-E1-D3 5243 1418 LIB36-002- LIB36 g22396 BLASTN 1505 1e−116 94 Q1-E1-E7 5244 1418 LIB36-012- LIB36 g22396 BLASTN 1241 1e−113 97 Q1-E1-F6 5245 1418 LIB189-032- LIB189 g22407 BLASTN 803 1e−106 92 Q1-E1-E4 5246 1418 LIB36-018- LIB36 g22396 BLASTN 916 1e−104 92 Q1-E1-H1 5247 1418 LIB3078-023- LIB3078 g22396 BLASTN 1052 1e−96 84 Q1-K1-H1 5248 1418 LIB3060-019- LIB3060 g22415 BLASTN 1109 1e−96 88 Q1-K1-E7 5249 1418 LIB3060-042- LIB3060 g22407 BLASTN 1236 1e−94 94 Q1-K1-E5 5250 1418 LIB3060-019- LIB3060 g22415 BLASTN 978 1e−92 75 Q1-K1-B3 5251 1418 LIB36-009- LIB36 g22396 BLASTN 1128 1e−90 98 Q1-E1-D2 5252 1418 LIB189-009- LIB189 g22407 BLASTN 1107 1e−89 96 Q1-E1-G7 5253 1418 LIB83-007- LIB83 g22396 BLASTN 1151 1e−86 99 Q1-E1-G12 5254 1418 LIB36-007- LIB36 g22396 BLASTN 1136 1e−85 99 Q1-E1-G7 5255 1418 LIB3060-004- LIB3060 g22415 BLASTN 521 1e−82 92 Q1-K1-C8 5256 1418 LIB3060-026- LIB3060 g22407 BLASTN 339 1e−76 81 Q1-K1-C11 5257 1418 LIB3060-022- LIB3060 g22407 BLASTN 845 1e−72 88 Q1-K1-G9 5258 1418 LIB189-029- LIB189 g22407 BLASTN 611 1e−67 93 Q1-E1-C4 5259 1418 LIB3060-019- LIB3060 g22407 BLASTN 389 1e−66 87 Q1-K1-E3 5260 1418 LIB36-004- LIB36 g22407 BLASTN 649 1e−62 83 Q1-E1-E2 5261 1418 LIB83-005- LIB83 g22396 BLASTN 656 1e−45 99 Q1-E1-A6 5262 1418 LIB84-026- LIB84 g22407 BLASTN 337 1e−43 89 Q1-E1-F1 5263 1418 LIB84-014- LIB84 g22396 BLASTN 435 1e−27 100 Q1-E1-A8 5264 1418 LIB36-021- LIB36 g22396 BLASTN 346 1e−19 99 Q1-E1-H5 5265 16592 LIB3060-041- LIB3060 g22415 BLASTN 1550 1e−173 99 Q1-K1-A12 5266 16592 LIB3060-007- LIB3060 g22562 BLASTN 2092 1e−165 98 Q1-K1-C8 5267 16592 LIB3060-014- LIB3060 g22562 BLASTN 2034 1e−160 96 Q1-K1-D4 5268 16592 LIB3060-029- LIB3060 g22562 BLASTN 1998 1e−157 97 Q1-K1-H6 5269 16592 LIB3060-011- LIB3060 g22562 BLASTN 1805 1e−155 96 Q1-K1-G8 5270 16592 LIB3060-007- LIB3060 g22562 BLASTN 1875 1e−155 94 Q1-K1-E2 5271 16592 LIB3060-003- LIB3060 g22415 BLASTN 1266 1e−135 89 Q1-K1-E9 5272 16592 LIB3060-026- LIB3060 g22415 BLASTN 1712 1e−133 91 Q1-K1-H9 5273 16592 LIB3060-020- LIB3060 g22412 BLASTN 699 1e−113 95 Q1-K1-F11 5274 201 LIB3067-017- LIB3067 g3132309 BLASTN 905 1e−98 81 Q1-K1-H10 5275 21797 LIB3067-036- LIB3067 g3132309 BLASTN 993 1e−117 89 Q1-K1-C4 5276 26948 LIB3069-056- LIB3069 g21629 BLASTN 273 1e−15 85 Q1-K1-C9 5277 26948 LIB36-004- LIB36 g21629 BLASTN 273 1e−14 83 Q1-E1-E1 5278 30586 LIB3067-044- LIB3067 g467551 BLASTN 1151 1e−87 79 Q1-K1-F10 5279 3591 LIB3059-005- LIB3059 g429148 BLASTN 2207 1e−174 99 Q1-K1-A6 5280 4329 LIB3060-051- LIB3060 g21629 BLASTN 1872 1e−147 91 Q1-K1-H4 5281 4530 LIB3059-014- LIB3059 g429148 BLASTN 2071 1e−163 98 Q1-K1-E8 5282 9226 LIB3069-044- LIB3069 g169843 BLASTN 1596 1e−123 89 Q1-K1-F2 SOYBEAN PHOSPHOENOLPYRUVATE CARBOXYLASE 5283 -700564927 700564927H1 SOYMON002 g218266 BLASTN 522 1e−79 95 5284 -700567858 700567858H1 SOYMON002 g2266946 BLASTN 892 1e−69 83 5285 -700648673 700648673H1 SOYMON003 g467551 BLASTN 1020 1e−106 97 5286 -700659068 700659068H1 SOYMON004 g218266 BLASTN 1095 1e−95 100 5287 -700728930 700728930H1 SOYMON009 g166416 BLASTX 114 1e−12 49 5288 -700739901 700739901H1 SOYMON012 g2266946 BLASTN 868 1e−63 81 5289 -700741179 700741179H1 SOYMON012 g2959439 BLASTX 190 1e−20 88 5290 -700742902 700742902H1 SOYMON012 g147341 BLASTX 71 1e−9 46 5291 -700751669 700751669H1 SOYMON014 g169844 BLASTX 263 1e−29 58 5292 -700753587 700753587H1 SOYMON014 g2266946 BLASTN 750 1e−53 81 5293 -700755512 700755512H1 SOYMON014 g218266 BLASTN 1173 1e−88 99 5294 -700755528 700755528H1 SOYMON014 g218266 BLASTN 623 1e−48 88 5295 -700834546 700834546H1 SOYMON019 g2266946 BLASTN 826 1e−59 85 5296 -700864136 700864136H1 SOYMON016 g2266946 BLASTN 637 1e−44 79 5297 -700876401 700876401H1 SOYMON018 g22560 BLASTN 540 1e−64 84 5298 -700890236 700890236H1 SOYMON024 g467551 BLASTN 491 1e−63 94 5299 -700955462 700955462H1 SOYMON022 g467551 BLASTN 521 1e−74 95 5300 -700959358 700959358H1 SOYMON022 g218266 BLASTN 1245 1e−94 100 5301 -700971291 700971291H1 SOYMON005 g218266 BLASTN 1307 1e−100 99 5302 -700979408 700979408H1 SOYMON009 g2266946 BLASTN 798 1e−70 85 5303 -700987250 700987250H1 SOYMON009 g2266946 BLASTN 656 1e−58 78 5304 -700987503 700987503H1 SOYMON009 g218266 BLASTN 890 1e−65 80 5305 -700991194 700991194H1 SOYMON011 g2266946 BLASTN 600 1e−41 78 5306 -701002203 701002203H1 SOYMON018 g2626748 BLASTN 420 1e−57 94 5307 -701043122 701043122H1 SOYMON029 g467551 BLASTN 823 1e−59 96 5308 -701043454 701043454H1 SOYMON029 g218266 BLASTN 631 1e−75 98 5309 -701046608 701046608H1 SOYMON032 g218266 BLASTN 891 1e−87 95 5310 -701062388 701062388H1 SOYMON033 g2626744 BLASTN 476 1e−40 93 5311 -701119910 701119910H1 SOYMON037 g2626742 BLASTN 630 1e−49 78 5312 -701213104 701213104H1 SOYMON035 g2266946 BLASTN 475 1e−57 78 5313 10663 700732365H1 SOYMON010 g2266946 BLASTN 875 1e−64 82 5314 10663 700981524H1 SOYMON009 g2266946 BLASTN 596 1e−62 80 5315 11125 700663617H1 SOYMON005 g218266 BLASTN 410 1e−38 98 5316 11125 700663717H1 SOYMON005 g218266 BLASTN 410 1e−35 85 5317 11125 700870993H1 SOYMON018 g218266 BLASTN 231 1e−9 96 5318 11227 700686116H1 SOYMON008 g2266946 BLASTN 995 1e−74 85 5319 11227 700944212H1 SOYMON024 g2266946 BLASTN 936 1e−69 85 5320 12325 700985848H1 SOYMON009 g2626742 BLASTN 1275 1e−97 94 5321 12325 701120339H1 SOYMON037 g467551 BLASTN 1210 1e−91 100 5322 12325 701214949H1 SOYMON035 g2626742 BLASTN 1175 1e−89 100 5323 12325 701096990H1 SOYMON028 g467551 BLASTN 1054 1e−78 94 5324 12325 701038039H1 SOYMON029 g467551 BLASTN 666 1e−77 98 5325 12325 701006212H2 SOYMON019 g467551 BLASTN 716 1e−62 95 5326 14728 700730704H1 SOYMON009 g2145426 BLASTX 147 1e−17 54 5327 14728 700685609H1 SOYMON008 g3341490 BLASTX 177 1e−17 43 5328 15298 701041573H1 SOYMON029 g2626742 BLASTN 1325 1e−101 100 5329 15298 701099785H1 SOYMON028 g2626742 BLASTN 1145 1e−100 100 5330 15298 700897382H1 SOYMON027 g2626742 BLASTN 972 1e−81 98 5331 17279 700874273H1 SOYMON018 g218266 BLASTN 980 1e−92 100 5332 17279 700684541H1 SOYMON008 g218266 BLASTN 328 1e−79 98 5333 18846 700836067H1 SOYMON019 g2626746 BLASTN 687 1e−97 99 5334 18846 700567643H1 SOYMON002 g2626746 BLASTN 1082 1e−83 99 5335 21305 700744392H1 SOYMON013 g19535 BLASTN 330 1e−33 78 5336 21305 700747092H1 SOYMON013 g19535 BLASTN 264 1e−28 80 5337 21695 700666285H1 SOYMON005 g218266 BLASTN 1251 1e−95 99 5338 21695 700945580H1 SOYMON024 g218266 BLASTN 1079 1e−81 88 5339 21940 701068565H1 SOYMON034 g218266 BLASTN 1334 1e−102 98 5340 21940 700943287H1 SOYMON024 g218266 BLASTN 945 1e−74 96 5341 22008 701040960H1 SOYMON029 g2626742 BLASTN 1321 1e−101 99 5342 22008 701038869H1 SOYMON029 g2626742 BLASTN 711 1e−66 99 5343 25805 700834887H1 SOYMON019 g2626742 BLASTN 1132 1e−85 95 5344 25805 701127019H1 SOYMON037 g467551 BLASTN 748 1e−80 96 5345 26379 701154209H1 SOYMON031 g2266946 BLASTN 799 1e−57 81 5346 26379 701154248H1 SOYMON031 g2626742 BLASTN 735 1e−52 81 5347 27397 701122563H1 SOYMON037 g2266946 BLASTN 753 1e−53 85 5348 27397 701122647H1 SOYMON037 g2266946 BLASTN 602 1e−41 76 5349 28129 701123443H1 SOYMON037 g1146155 BLASTX 102 1e−14 58 5350 6467 700648723H1 SOYMON003 g1213341 BLASTX 165 1e−19 68 5351 6467 700648341H1 SOYMON003 g1146154 BLASTN 257 1e−12 74 5352 7471 700889346H1 SOYMON024 g2266946 BLASTN 921 1e−67 85 5353 7471 700741422H1 SOYMON012 g2266946 BLASTN 891 1e−65 85 5354 7951 700962862H1 SOYMON022 g467551 BLASTN 1236 1e−94 99 5355 7951 700729127H1 SOYMON009 g467551 BLASTN 665 1e−93 100 5356 7951 700962754H1 SOYMON022 g467551 BLASTN 1127 1e−87 94 5357 9942 701042717H1 SOYMON029 g2626742 BLASTN 1275 1e−97 100 5358 9942 700943121H1 SOYMON024 g467551 BLASTN 1243 1e−94 99 5359 -GM12190 LIB3049-036- LIB3049 g18463 BLASTN 319 1e−16 69 Q1-E1-F5 5360 -GM13015 LIB3049-037- LIB3049 g18463 BLASTN 248 1e−11 74 Q1-E1-D7 5361 -GM13035 LIB3049-037- LIB3049 g18463 BLASTN 250 1e−11 65 Q1-E1-A8 5362 -GM13114 LIB3049-037- LIB3049 g18463 BLASTN 239 1e−9 63 Q1-E1-E12 5363 -GM13510 LIB3049-046- LIB3049 g2959438 BLASTN 531 1e−33 88 Q1-E1-A2 5364 -GM13784 LIB3049-048- LIB3049 g18463 BLASTN 242 1e−9 62 Q1-E1-E12 5365 -GM13839 LIB3049-051- LIB3049 g18463 BLASTN 230 1e−10 60 Q1-E1-C6 5366 -GM14450 LIB3049-056- LIB3049 g18463 BLASTN 231 1e−8 61 Q1-E1-D1 5367 -GM24091 LIB3040-011- LIB3040 g18463 BLASTN 221 1e−9 66 Q1-E1-G3 5368 -GM2515 LIB3028-013- LIB3028 g18463 BLASTN 242 1e−11 66 Q1-B1-H1 5369 -GM6973 LIB3039-025- LIB3039 g18463 BLASTN 240 1e−11 66 Q1-E1-C6 5370 -GM7231 LIB3039-024- LIB3039 g18463 BLASTN 264 1e−12 65 Q1-E1-C7 5371 12325 LIB3056-009- LIB3056 g467551 BLASTN 1487 1e−123 93 Q1-N1-H12 MAIZE NADP-DEPENDENT MALATE DEHYDROGENASE 5372 -700579267 700579267H1 SATMON031 g22367 BLASTN 472 1e−43 88 5373 4577 700098054H1 SATMON009 g22367 BLASTN 835 1e−121 100 5374 4577 700097706H1 SATMON009 g22367 BLASTN 1536 1e−119 98 5375 4577 700097409H1 SATMON009 g22367 BLASTN 1497 1e−116 98 5376 4577 700100389H1 SATMON009 g22367 BLASTN 1431 1e−110 98 5377 4577 700098228H1 SATMON009 g22367 BLASTN 1405 1e−108 93 5378 4577 700042625H1 SATMON004 g22367 BLASTN 1366 1e−105 99 5379 4577 700044532H1 SATMON004 g22367 BLASTN 1366 1e−105 99 5380 4577 700426221H1 SATMONN01 g22367 BLASTN 761 1e−103 98 5381 4577 700045403H1 SATMON004 g22367 BLASTN 1145 1e−103 100 5382 4577 700100550H1 SATMON009 g22367 BLASTN 747 1e−101 97 5383 4577 700439608H1 SATMON026 g22367 BLASTN 1187 1e−100 97 5384 4577 700578318H1 SATMON031 g22367 BLASTN 755 1e−97 98 5385 4577 700084313H1 SATMON011 g22367 BLASTN 589 1e−96 98 5386 4577 700434067H1 SATMONN01 g22367 BLASTN 697 1e−95 98 5387 4577 700578011H1 SATMON031 g22367 BLASTN 1125 1e−93 99 5388 4577 700099962H1 SATMON009 g22367 BLASTN 1231 1e−93 87 5389 4577 700445309H1 SATMON027 g22367 BLASTN 452 1e−92 96 5390 4577 700213872H1 SATMON016 g22367 BLASTN 1181 1e−89 92 5391 4577 700578418H1 SATMON031 g22367 BLASTN 981 1e−85 95 5392 4577 700429351H1 SATMONN01 g22367 BLASTN 624 1e−84 96 5393 4577 700045012H1 SATMON004 g22367 BLASTN 1125 1e−84 94 5394 4577 700197938H1 SATMON016 g22367 BLASTN 1108 1e−83 99 5395 4577 700433880H1 SATMONN01 g22367 BLASTN 755 1e−73 97 5396 4577 700043693H1 SATMON004 g22367 BLASTN 886 1e−73 95 5397 4577 700581629H1 SATMON031 g22367 BLASTN 335 1e−69 91 5398 4577 700422827H1 SATMONN01 g22367 BLASTN 831 1e−69 96 5399 4577 700167037H1 SATMON013 g22367 BLASTN 889 1e−65 94 5400 4577 700438770H1 SATMON026 g22367 BLASTN 666 1e−53 94 5401 4577 700425253H1 SATMONN01 g22367 BLASTN 436 1e−50 95 5402 4577 700423354H1 SATMONN01 g22367 BLASTN 462 1e−50 97 5403 4577 700211538H1 SATMON016 g22367 BLASTN 540 1e−43 100 5404 4577 700097126H1 SATMON009 g22367 BLASTN 504 1e−33 97 5405 4577 700098826H1 SATMON009 g22367 BLASTN 488 1e−31 90 5406 4577 700100862H1 SATMON009 g22367 BLASTN 189 1e−13 92 5407 -L30602059 LIB3060-016- LIB3060 g22367 BLASTN 838 1e−128 87 Q1-K1-C12 5408 4577 LIB36-016- LIB36 g22367 BLASTN 2081 1e−164 98 Q2-E2-D10 5409 4577 LIB3078-033- LIB3078 g22367 BLASTN 2048 1e−162 93 Q1-K1-F11 5410 4577 LIB36-013- LIB36 g22367 BLASTN 2051 1e−162 97 Q1-E1-D5 5411 4577 LIB3060-021- LIB3060 g22367 BLASTN 1589 1e−156 96 Q1-K1-F9 5412 4577 LIB36-015- LIB36 g22367 BLASTN 1805 1e−153 98 Q1-E1-A7 5413 4577 LIB36-002- LIB36 g22367 BLASTN 1723 1e−149 91 Q1-E1-D3 5414 4577 LIB3060-013- LIB3060 g22367 BLASTN 1836 1e−149 96 Q1-K1-G5 5415 4577 LIB3060-013- LIB3060 g22367 BLASTN 1091 1e−135 95 Q1-K1-G2 5416 4577 LIB36-020- LIB36 g22367 BLASTN 1400 1e−130 96 Q1-E1-F1 5417 4577 LIB3079-013- LIB3079 g22367 BLASTN 1474 1e−128 98 Q1-K1-G10 5418 4577 LIB189-018- LIB189 g22367 BLASTN 1427 1e−125 93 Q1-E1-C10 5419 4577 LIB3078-052- LIB3078 g22367 BLASTN 1306 1e−114 90 Q1-K1-B9 SOYBEAN NADP-DEPENDENT MALATE DEHYDROGENASE 5420 -701120823 701120823H1 SOYMON037 g397474 BLASTN 410 1e−52 84 5421 13458 700897079H1 SOYMON027 g397474 BLASTN 874 1e−64 83 5422 5228 701139976H1 SOYMON038 g397474 BLASTN 1145 1e−86 92 5423 5228 700738591H1 SOYMON012 g397474 BLASTN 991 1e−73 91 MAIZE ASPARTATE AMINOTRANSFERASE 5424 -700028003 700028003H1 SATMON003 g63066 BLASTX 125 1e−10 79 5425 -700072842 700072842H1 SATMON007 g1001121 BLASTX 259 1e−28 50 5426 -700194011 700194011H1 SATMON014 g435456 BLASTN 324 1e−18 73 5427 -700196486 700196486H1 SATMON014 g20599 BLASTX 68 1e−10 74 5428 -700331820 700331820H1 SATMON019 g20600 BLASTN 1192 1e−90 90 5429 -700454550 700454550H1 SATMON029 g435458 BLASTN 198 1e−20 82 5430 -700454567 700454567H1 SATMON029 g435458 BLASTN 333 1e−24 82 5431 -700454642 700454642H1 SATMON029 g435458 BLASTN 269 1e−23 89 5432 -700454849 700454849H1 SATMON029 g435458 BLASTN 318 1e−26 87 5433 -700468560 700468560H1 SATMON025 g3328816 BLASTX 139 1e−19 58 5434 -700476413 700476413H1 SATMON025 g2984217 BLASTX 156 1e−22 52 5435 -700615109 700615109H1 SATMON033 g20598 BLASTN 256 1e−17 81 5436 -701161385 701161385H1 SATMONN04 g435458 BLASTN 523 1e−45 80 5437 10165 700341126H1 SATMON020 g20596 BLASTN 743 1e−71 91 5438 10165 700160220H1 SATMON012 g20596 BLASTN 769 1e−55 92 5439 10165 700158802H1 SATMON012 g20596 BLASTN 617 1e−42 94 5440 10192 700204319H1 SATMON003 g2984217 BLASTX 148 1e−13 55 5441 10329 700095671H1 SATMON008 g20600 BLASTN 816 1e−59 87 5442 10329 700214146H1 SATMON016 g20596 BLASTN 610 1e−42 88 5443 10329 700041823H1 SATMON004 g20596 BLASTN 615 1e−42 78 5444 10329 700094321H1 SATMON008 g20596 BLASTN 559 1e−40 88 5445 1148 700089060H1 SATMON011 g633094 BLASTN 1397 1e−107 92 5446 1148 700044414H1 SATMON004 g633094 BLASTN 1272 1e−97 92 5447 1148 700101429H1 SATMON009 g633094 BLASTN 1221 1e−92 91 5448 1148 700221366H1 SATMON011 g633094 BLASTN 1205 1e−91 94 5449 1148 700101604H1 SATMON009 g633094 BLASTN 1167 1e−88 89 5450 1148 700041864H1 SATMON004 g633094 BLASTN 1159 1e−87 91 5451 1148 700157048H1 SATMON012 g633094 BLASTN 1121 1e−84 93 5452 1148 700581463H1 SATMON031 g633094 BLASTN 1124 1e−84 90 5453 1148 700579938H1 SATMON031 g633094 BLASTN 661 1e−83 91 5454 1148 700432477H1 SATMONN01 g633094 BLASTN 1050 1e−78 90 5455 1148 700154706H1 SATMON007 g633094 BLASTN 997 1e−74 90 5456 1148 700043761H1 SATMON004 g633094 BLASTN 905 1e−66 92 5457 1148 700423679H1 SATMONN01 g633094 BLASTN 555 1e−54 81 5458 1148 700424076H1 SATMONN01 g633094 BLASTN 228 1e−19 87 5459 1148 701166426H1 SATMONN04 g633094 BLASTN 221 1e−16 79 5460 16872 700211160H1 SATMON016 g633094 BLASTN 482 1e−56 88 5461 16872 700043705H1 SATMON004 g633094 BLASTN 293 1e−42 85 5462 16872 700208983H1 SATMON016 g633094 BLASTN 250 1e−15 84 5463 16872 700101375H1 SATMON009 g633094 BLASTN 154 1e−11 87 5464 17829 700581970H1 SATMON031 g1001309 BLASTX 107 1e−11 53 5465 17829 700194282H1 SATMON014 g1001309 BLASTX 107 1e−11 53 5466 18047 700206971H1 SATMON003 g1103380 BLASTX 107 1e−12 53 5467 19241 700472363H1 SATMON025 g20598 BLASTN 1010 1e−81 89 5468 19241 700472263H1 SATMON025 g20598 BLASTN 916 1e−78 89 5469 19241 700806145H1 SATMON036 g20598 BLASTN 947 1e−74 92 5470 319 700076939H1 SATMON007 g20598 BLASTN 1102 1e−83 89 5471 319 700349974H1 SATMON023 g20598 BLASTN 1018 1e−80 84 5472 319 700235923H1 SATMON010 g20598 BLASTN 1017 1e−79 88 5473 319 700206180H1 SATMON003 g20598 BLASTN 838 1e−78 86 5474 319 700476547H1 SATMON025 g20598 BLASTN 794 1e−76 88 5475 319 700258893H1 SATMON017 g20598 BLASTN 897 1e−73 89 5476 319 700612236H1 SATMON022 g20598 BLASTN 820 1e−72 86 5477 319 700806537H1 SATMON036 g20598 BLASTN 949 1e−70 87 5478 319 700450338H1 SATMON028 g20598 BLASTN 912 1e−67 85 5479 319 700806243H1 SATMON036 g20598 BLASTN 782 1e−66 87 5480 319 700263732H1 SATMON017 g435456 BLASTN 662 1e−61 86 5481 319 700806094H1 SATMON036 g20598 BLASTN 375 1e−59 91 5482 319 700152610H1 SATMON007 g20598 BLASTN 806 1e−58 85 5483 319 700614581H1 SATMON033 g20598 BLASTN 729 1e−51 89 5484 319 700349161H1 SATMON023 g20598 BLASTN 270 1e−30 87 5485 319 700805964H1 SATMON036 g20598 BLASTN 463 1e−29 79 5486 319 700450544H1 SATMON028 g20598 BLASTN 280 1e−27 86 5487 319 700618252H1 SATMON033 g20598 BLASTN 407 1e−26 86 5488 319 700615189H1 SATMON033 g20598 BLASTN 309 1e−25 87 5489 319 700264196H1 SATMON017 g20598 BLASTN 412 1e−25 84 5490 4431 700211615H1 SATMON016 g1001309 BLASTX 96 1e−9 32 5491 541 700073508H1 SATMON007 g633094 BLASTN 1388 1e−106 91 5492 541 700098793H1 SATMON009 g633094 BLASTN 1329 1e−101 90 5493 541 700101956H1 SATMON009 g633094 BLASTN 1307 1e−100 89 5494 541 700100132H1 SATMON009 g633094 BLASTN 1314 1e−100 93 5495 541 700799335H1 SATMON036 g633094 BLASTN 1216 1e−92 95 5496 541 700446909H1 SATMON027 g633094 BLASTN 1154 1e−87 91 5497 541 700444305H1 SATMON027 g633094 BLASTN 988 1e−86 97 5498 541 700222187H1 SATMON011 g633094 BLASTN 1116 1e−84 89 5499 541 700093340H1 SATMON008 g633094 BLASTN 1121 1e−84 90 5500 541 700576310H1 SATMON030 g633094 BLASTN 1107 1e−83 91 5501 541 700443474H1 SATMON027 g633094 BLASTN 584 1e−82 93 5502 541 700440955H1 SATMON026 g633094 BLASTN 803 1e−82 92 5503 541 700446111H1 SATMON027 g633094 BLASTN 939 1e−81 87 5504 541 700259835H1 SATMON017 g633094 BLASTN 1073 1e−80 87 5505 541 700551206H1 SATMON022 g633094 BLASTN 968 1e−76 89 5506 541 700445905H1 SATMON027 g633094 BLASTN 464 1e−75 89 5507 541 700446192H1 SATMON027 g633094 BLASTN 774 1e−55 92 5508 541 700614693H1 SATMON033 g633094 BLASTN 600 1e−54 80 5509 7402 700439746H1 SATMON026 g20596 BLASTN 1353 1e−103 97 5510 7402 700621225H1 SATMON034 g20596 BLASTN 709 1e−72 97 5511 7402 700456918H1 SATMON029 g20596 BLASTN 968 1e−71 95 5512 7402 700453876H1 SATMON029 g20600 BLASTN 761 1e−54 96 5513 7402 700623616H1 SATMON034 g20596 BLASTN 432 1e−39 96 5514 7402 700454592H1 SATMON029 g20600 BLASTN 380 1e−30 81 5515 7402 700454593H1 SATMON029 g20600 BLASTN 310 1e−28 96 5516 7482 700197666H1 SATMON014 g2621088 BLASTX 145 1e−24 55 5517 7482 700615228H1 SATMON033 g3328816 BLASTX 201 1e−20 61 5518 7482 700030129H1 SATMON003 g3328816 BLASTX 178 1e−17 56 5519 7482 700579227H1 SATMON031 g2621088 BLASTX 132 1e−15 44 5520 786 700476002H1 SATMON025 g20598 BLASTN 1119 1e−90 92 5521 786 700461103H1 SATMON033 g20598 BLASTN 1196 1e−90 91 5522 786 700240702H1 SATMON010 g20598 BLASTN 1174 1e−89 91 5523 786 700470851H1 SATMON025 g20598 BLASTN 1138 1e−86 91 5524 786 700262654H1 SATMON017 g20598 BLASTN 1138 1e−86 91 5525 786 700452647H1 SATMON028 g20598 BLASTN 1115 1e−84 88 5526 786 700194349H1 SATMON014 g20598 BLASTN 1115 1e−84 92 5527 786 700472225H1 SATMON025 g20598 BLASTN 645 1e−82 86 5528 786 700461203H1 SATMON033 g20598 BLASTN 1019 1e−82 90 5529 786 700581588H1 SATMON031 g20598 BLASTN 561 1e−79 90 5530 786 700194330H1 SATMON014 g20598 BLASTN 1043 1e−78 90 5531 786 700194016H1 SATMON014 g20598 BLASTN 1044 1e−78 90 5532 786 700157347H1 SATMON012 g20598 BLASTN 1049 1e−78 90 5533 786 700195805H1 SATMON014 g20598 BLASTN 1049 1e−78 90 5534 786 700160255H1 SATMON012 g20598 BLASTN 1040 1e−77 93 5535 786 700582138H1 SATMON031 g20598 BLASTN 885 1e−75 88 5536 786 700197148H1 SATMON014 g20598 BLASTN 1007 1e−75 90 5537 786 700159366H1 SATMON012 g20598 BLASTN 1016 1e−75 91 5538 786 701184326H1 SATMONN06 g20598 BLASTN 815 1e−72 89 5539 786 700159491H1 SATMON012 g20598 BLASTN 979 1e−72 93 5540 786 700104663H1 SATMON010 g20598 BLASTN 966 1e−71 86 5541 786 700195003H1 SATMON014 g20598 BLASTN 779 1e−69 86 5542 786 700218254H1 SATMON016 g20598 BLASTN 942 1e−69 89 5543 786 700802451H1 SATMON036 g20598 BLASTN 581 1e−68 90 5544 786 700157772H1 SATMON012 g20598 BLASTN 887 1e−65 90 5545 786 700473425H1 SATMON025 g20598 BLASTN 466 1e−64 85 5546 786 700800486H1 SATMON036 g20598 BLASTN 868 1e−63 91 5547 786 700185039H1 SATMON014 g20598 BLASTN 859 1e−62 86 5548 786 700800057H1 SATMON036 g20598 BLASTN 567 1e−59 85 5549 786 700451832H1 SATMON028 g20598 BLASTN 501 1e−58 88 5550 786 700799994H1 SATMON036 g20598 BLASTN 570 1e−55 91 5551 786 700801486H1 SATMON036 g20598 BLASTN 750 1e−53 91 5552 786 700802086H1 SATMON036 g20598 BLASTN 459 1e−51 89 5553 786 700477105H1 SATMON025 g20598 BLASTN 708 1e−50 90 5554 786 700260426H1 SATMON017 g20598 BLASTN 702 1e−49 84 5555 786 700799811H1 SATMON036 g20598 BLASTN 409 1e−48 84 5556 786 700427005H1 SATMONN01 g20598 BLASTN 691 1e−48 89 5557 786 700803487H1 SATMON036 g20598 BLASTN 423 1e−46 83 5558 786 700262695H1 SATMON017 g20598 BLASTN 367 1e−43 89 5559 786 700471602H1 SATMON025 g20598 BLASTN 601 1e−41 90 5560 786 701185813H2 SATMONN06 g20598 BLASTN 320 1e−39 83 5561 786 700196744H1 SATMON014 g20598 BLASTN 490 1e−32 92 5562 786 701184204H1 SATMONN06 g20598 BLASTN 247 1e−10 78 5563 786 700622453H1 SATMON034 g20598 BLASTN 230 1e−8 79 5564 786 700618768H1 SATMON034 g20598 BLASTN 230 1e−8 79 5565 -L30591931 LIB3059-009- LIB3059 g20596 BLASTN 1989 1e−157 95 Q1-K1-C12 5566 -L30593805 LIB3059-022- LIB3059 g20596 BLASTN 377 1e−56 79 Q1-K1-H6 5567 -L30596704 LIB3059-055- LIB3059 g20596 BLASTN 733 1e−52 89 Q1-K1-E5 5568 -L30624957 LIB3062-040- LIB3062 g633095 BLASTX 112 1e−27 56 Q1-K1-H1 5569 -L30671766 LIB3067-014- LIB3067 g20596 BLASTN 1132 1e−122 86 Q1-K1-B8 5570 -L30693715 LIB3069-012- LIB3069 g142538 BLASTX 98 1e−24 47 Q1-K1-F3 5571 10329 LIB3079-007- LIB3079 g20596 BLASTN 1201 1e−97 87 Q1-K1-B3 5572 10329 LIB143-052- LIB143 g20596 BLASTN 751 1e−53 86 Q1-E1-E4 5573 1148 LIB3078-040- LIB3078 g633094 BLASTN 1675 1e−130 87 Q1-K1-H1 5574 1148 LIB3062-040- LIB3062 g633094 BLASTN 1310 1e−100 88 Q1-K1-H3 5575 1148 LIB143-054- LIB143 g633094 BLASTN 1234 1e−94 88 Q1-E1-F1 5576 1148 LIB83-001- LIB83 g633094 BLASTN 1030 1e−77 81 Q1-E1-A10 5577 16872 LIB36-018- LIB36 g633094 BLASTN 542 1e−69 85 Q1-E1-D12 5578 25099 LIB3059-012- LIB3059 g1001309 BLASTX 130 1e−36 38 Q1-K1-G3 5579 319 LIB143-022- LIB143 g20598 BLASTN 1698 1e−135 89 Q1-E1-G3 5580 319 LIB143-048- LIB143 g20598 BLASTN 1562 1e−126 87 Q1-E1-G12 5581 319 LIB143-001- LIB143 g20598 BLASTN 1462 1e−113 90 Q1-E1-H6 5582 319 LIB143-002- LIB143 g20598 BLASTN 484 1e−66 88 Q1-E1-H2 5583 32047 LIB148-034- LIB148 g435456 BLASTN 262 1e−12 68 Q1-E1-F3 5584 32047 LIB148-032- LIB148 g435456 BLASTN 255 1e−11 71 Q1-E1-H8 5585 541 LIB3062-033- LIB3062 g633094 BLASTN 1706 1e−133 90 Q1-K1-G2 5586 541 LIB3062-033- LIB3062 g633094 BLASTN 1123 1e−94 84 Q1-K1-G3 5587 541 LIB3060-005- LIB3060 g633094 BLASTN 1061 1e−90 84 Q1-K1-C1 5588 7402 LIB3059-004- LIB3059 g20596 BLASTN 1461 1e−142 92 Q1-K1-F4 5589 786 LIB3061-042- LIB3061 g20598 BLASTN 1811 1e−142 88 Q1-K1-E8 5590 786 LIB143-040- LIB143 g20598 BLASTN 1462 1e−113 92 Q1-E1-D11 5591 786 LIB143-030- LIB143 g20598 BLASTN 1141 1e−101 90 Q1-E1-D9 5592 786 LIB3068-035- LIB3068 g20598 BLASTN 533 1e−99 78 Q1-K1-A4 5593 786 LIB143-017- LIB143 g20598 BLASTN 678 1e−92 82 Q1-E1-C8 5594 786 LIB143-030- LIB143 g20598 BLASTN 1165 1e−88 86 Q1-E1-D11 5595 786 LIB3061-048- LIB3061 g20598 BLASTN 299 1e−15 78 Q1-K1-D7 5596 786 LIB3059-056- LIB3059 g20598 BLASTN 283 1e−12 74 Q1-K1-B1 MAIZE PUTATIVE ASPARTATE AMINOTRANSFERASE 5597 -700201453 700201453H1 SATMON003 g1049345 BLASTX 178 1e−17 64 5598 23836 700243862H1 SATMON010 g1778518 BLASTX 133 1e−11 49 5599 23836 701169557H1 SATMONN05 g1778518 BLASTX 126 1e−10 54 5600 7482 LIB3059-049- LIB3059 g2621088 BLASTX 138 1e−48 51 Q1-K1-E5 SOYBEAN ASPARTATE AMINOTRANSFERASE 5601 -700668054 700668054H1 SOYMON006 g3328816 BLASTX 172 1e−16 53 5602 -700685655 700685655H1 SOYMON008 g387106 BLASTX 165 1e−15 62 5603 -700729138 700729138H1 SOYMON009 g2621088 BLASTX 136 1e−17 47 5604 -700734818 700734818H1 SOYMON010 g3201622 BLASTX 234 1e−25 54 5605 -700787411 700787411H2 SOYMON011 g20598 BLASTN 908 1e−66 90 5606 -700868646 700868646H1 SOYMON016 g435458 BLASTN 513 1e−33 75 5607 -700874369 700874369H1 SOYMON018 g2654093 BLASTN 808 1e−63 90 5608 -700974412 700974412H1 SOYMON005 g169914 BLASTN 249 1e−11 83 5609 -701009475 701009475H1 SOYMON019 g1001309 BLASTX 111 1e−15 49 5610 -701050301 701050301H1 SOYMON032 g169914 BLASTN 263 1e−11 75 5611 -701061267 701061267H1 SOYMON033 g169914 BLASTN 235 1e−35 88 5612 -701129551 701129551H1 SOYMON037 g169914 BLASTN 1232 1e−93 93 5613 13413 700904367H1 SOYMON022 g1001121 BLASTX 231 1e−24 52 5614 13413 700895714H1 SOYMON027 g2266762 BLASTX 175 1e−22 49 5615 13413 700727795H1 SOYMON009 g1001121 BLASTX 190 1e−19 48 5616 13503 700974712H1 SOYMON005 g169914 BLASTN 1358 1e−104 99 5617 13503 700895483H1 SOYMON027 g169914 BLASTN 1236 1e−94 97 5618 13503 700846207H1 SOYMON021 g169914 BLASTN 1136 1e−85 94 5619 14358 700909477H1 SOYMON022 g710595 BLASTN 1309 1e−100 98 5620 14358 700732673H1 SOYMON010 g710595 BLASTN 1296 1e−99 98 5621 14358 700890192H1 SOYMON024 g710595 BLASTN 913 1e−83 98 5622 14358 700727008H1 SOYMON009 g710595 BLASTN 553 1e−55 99 5623 15432 700567458H1 SOYMON002 g1001309 BLASTX 115 1e−8 31 5624 15529 701045375H1 SOYMON032 g3201622 BLASTX 189 1e−19 55 5625 15529 700567374H1 SOYMON002 g3201622 BLASTX 186 1e−18 55 5626 15529 701102885H1 SOYMON028 g3201622 BLASTX 172 1e−16 56 5627 15529 701213187H1 SOYMON035 g3201622 BLASTX 174 1e−16 55 5628 15529 701055675H1 SOYMON032 g3201622 BLASTX 166 1e−15 60 5629 15529 701052631H1 SOYMON032 g3201622 BLASTX 159 1e−14 53 5630 15529 701213639H1 SOYMON035 g3201622 BLASTX 110 1e−13 59 5631 1566 700651242H1 SOYMON003 g2654093 BLASTN 1433 1e−146 98 5632 1566 700661083H1 SOYMON005 g2654093 BLASTN 898 1e−102 95 5633 1566 700668434H1 SOYMON006 g2654093 BLASTN 1289 1e−98 99 5634 1566 700677640H1 SOYMON007 g2654093 BLASTN 758 1e−97 99 5635 1566 700655909H1 SOYMON004 g2654093 BLASTN 730 1e−95 100 5636 1566 700660728H1 SOYMON005 g2654093 BLASTN 634 1e−81 90 5637 1566 700807523H1 SOYMON016 g2654093 BLASTN 478 1e−31 87 5638 16634 700660070H1 SOYMON004 g2621088 BLASTX 111 1e−20 54 5639 16634 700746670H1 SOYMON013 g2621088 BLASTX 118 1e−18 53 5640 1703 700749933H1 SOYMON013 g2654093 BLASTN 1385 1e−106 100 5641 1703 700793749H1 SOYMON017 g2654093 BLASTN 1370 1e−105 100 5642 1703 701127031H1 SOYMON037 g2654093 BLASTN 716 1e−94 96 5643 1703 700997259H1 SOYMON018 g2654093 BLASTN 1089 1e−81 97 5644 1703 700670783H1 SOYMON006 g2654093 BLASTN 767 1e−79 93 5645 25132 700678487H1 SOYMON007 g2654093 BLASTN 1175 1e−104 98 5646 25132 701049020H1 SOYMON032 g2654093 BLASTN 1260 1e−96 100 5647 25542 701151325H1 SOYMON031 g1001309 BLASTX 96 1e−15 51 5648 25542 700964436H1 SOYMON022 g1001309 BLASTX 107 1e−13 51 5649 26671 701106241H1 SOYMON036 g1001309 BLASTX 121 1e−9 39 5650 26671 701149504H1 SOYMON031 g1001309 BLASTX 122 1e−9 36 5651 27066 700605347H2 SOYMON004 g169914 BLASTN 1147 1e−104 99 5652 27066 701053078H1 SOYMON032 g169914 BLASTN 833 1e−87 96 5653 6297 700971234H1 SOYMON005 g169914 BLASTN 1303 1e−99 99 5654 6297 701205146H1 SOYMON035 g169914 BLASTN 1269 1e−96 94 5655 6297 701137753H1 SOYMON038 g169914 BLASTN 335 1e−85 93 5656 6297 700741154H1 SOYMON012 g169914 BLASTN 1135 1e−85 100 5657 6297 700954813H1 SOYMON022 g169914 BLASTN 1095 1e−84 100 5658 6297 701000832H1 SOYMON018 g169914 BLASTN 410 1e−83 95 5659 6297 701039262H1 SOYMON029 g169914 BLASTN 650 1e−82 97 5660 6297 701108365H1 SOYMON036 g169914 BLASTN 1032 1e−80 97 5661 6297 700953963H1 SOYMON022 g169914 BLASTN 1058 1e−79 92 5662 6297 700971364H1 SOYMON005 g169914 BLASTN 865 1e−63 95 5663 6297 701002832H1 SOYMON019 g169914 BLASTN 599 1e−62 90 5664 6297 700650013H1 SOYMON003 g169914 BLASTN 686 1e−61 88 5665 6297 701139166H1 SOYMON038 g169914 BLASTN 632 1e−43 83 5666 6297 701055975H1 SOYMON032 g169914 BLASTN 611 1e−42 99 5667 6297 701131513H1 SOYMON038 g169914 BLASTN 600 1e−41 96 5668 6297 701065138H1 SOYMON034 g169914 BLASTN 432 1e−38 89 5669 6297 701010254H2 SOYMON019 g169914 BLASTN 427 1e−36 88 5670 7549 700666429H1 SOYMON005 g169914 BLASTN 1249 1e−95 96 5671 7549 701001911H1 SOYMON018 g169914 BLASTN 819 1e−59 98 5672 7585 701127651H1 SOYMON037 g2654093 BLASTN 1360 1e−104 100 5673 7585 700668614H1 SOYMON006 g2654093 BLASTN 1341 1e−102 99 5674 7585 701054030H1 SOYMON032 g2654093 BLASTN 1341 1e−102 99 5675 7585 700890128H1 SOYMON024 g2654093 BLASTN 1285 1e−98 100 5676 7585 701056607H1 SOYMON032 g2654093 BLASTN 1069 1e−96 96 5677 7585 700973306H1 SOYMON005 g2654093 BLASTN 1250 1e−95 100 5678 7585 700845404H1 SOYMON021 g2654093 BLASTN 890 1e−94 96 5679 7585 700650253H1 SOYMON003 g2654093 BLASTN 1232 1e−93 98 5680 7585 700672829H1 SOYMON006 g2654093 BLASTN 1188 1e−90 99 5681 7585 700664509H1 SOYMON005 g2654093 BLASTN 1074 1e−87 97 5682 7585 701056892H1 SOYMON032 g2654093 BLASTN 1158 1e−87 93 5683 7585 700605686H2 SOYMON005 g2654093 BLASTN 1048 1e−86 97 5684 7585 700894006H1 SOYMON024 g2654093 BLASTN 1052 1e−85 96 5685 7585 700955412H1 SOYMON022 g2654093 BLASTN 625 1e−84 95 5686 7585 700560909H1 SOYMON001 g2654093 BLASTN 1119 1e−84 93 5687 7585 700895972H1 SOYMON027 g2654093 BLASTN 1105 1e−83 100 5688 7585 700663309H1 SOYMON005 g2654093 BLASTN 888 1e−82 95 5689 7585 700787774H2 SOYMON011 g2654093 BLASTN 943 1e−82 96 5690 7585 701069589H1 SOYMON034 g2654093 BLASTN 539 1e−81 93 5691 7585 700663096H1 SOYMON005 g2654093 BLASTN 498 1e−80 95 5692 7585 700836390H1 SOYMON020 g2654093 BLASTN 898 1e−80 95 5693 7585 700967858H1 SOYMON033 g2654093 BLASTN 978 1e−80 92 5694 7585 701101575H1 SOYMON028 g2654093 BLASTN 1032 1e−80 97 5695 7585 700750565H1 SOYMON014 g2654093 BLASTN 812 1e−79 95 5696 7585 701064276H1 SOYMON034 g2654093 BLASTN 820 1e−75 90 5697 7585 700995223H1 SOYMON011 g2654093 BLASTN 765 1e−68 89 5698 7585 700756072H1 SOYMON014 g2654093 BLASTN 899 1e−66 93 5699 7585 701147945H1 SOYMON031 g2654093 BLASTN 648 1e−64 95 5700 7585 700888603H1 SOYMON024 g2654093 BLASTN 865 1e−63 96 5701 9138 700562918H1 SOYMON002 g152149 BLASTX 195 1e−26 61 5702 9138 700654444H1 SOYMON004 g152149 BLASTX 191 1e−24 60 5703 9138 701037102H1 SOYMON029 g152149 BLASTX 123 1e−16 53 5704 -GM17331 LIB3055-010- LIB3055 g169914 BLASTN 456 1e−27 85 Q1-N1-G4 5705 -GM25144 LIB3040-027- LIB3040 g2654093 BLASTN 526 1e−65 85 Q1-E1-F2 5706 -GM41298 LIB3051-109- LIB3051 g2654093 BLASTN 207 1e−29 83 Q1-K1-F6 5707 14358 LIB3051-106- LIB3051 g710595 BLASTN 2246 1e−178 99 Q1-K1-G8 5708 25132 LIB3051-063- LIB3051 g2654093 BLASTN 1347 1e−103 96 Q1-K1-D12 5709 3196 LIB3065-006- LIB3065 g1778518 BLASTX 170 1e−32 50 Q1-N1-B10 5710 32509 LIB3056-012- LIB3056 g2648397 BLASTX 152 1e−29 43 Q1-N1-C3 5711 6297 LIB3055-010- LIB3055 g169914 BLASTN 1721 1e−134 99 Q1-N1-G6 5712 6297 LIB3055-010- LIB3055 g169914 BLASTN 1246 1e−123 97 Q1-N1-G7 5713 6297 LIB3055-010- LIB3055 g169914 BLASTN 1120 1e−84 93 Q1-N1-G8 5714 6297 LIB3049-021- LIB3049 g169914 BLASTN 864 1e−63 91 Q1-E1-C8 5715 7585 LIB3051-105- LIB3051 g2654093 BLASTN 2108 1e−167 99 Q1-K1-F8 5716 7585 LIB3028-010- LIB3028 g2654093 BLASTN 1973 1e−158 97 Q1-B1-C7 5717 7585 LIB3030-001- LIB3030 g2654093 BLASTN 1117 1e−138 95 Q1-B1-B7 5718 7585 LIB3051-040- LIB3051 g2654093 BLASTN 1166 1e−116 94 Q1-K1-D4 5719 9138 LIB3065-001- LIB3065 g152149 BLASTX 168 1e−38 52 Q1-N1-G1 SOYBEAN PUTATIVE ASPARTATE AMINOTRANSFERASE 5720 9138 700830720H1 SOYMON019 g3257794 BLASTX 186 1e−27 58 5721 9138 701100721H1 SOYMON028 g3257794 BLASTX 206 1e−23 56 5722 9138 700958391H1 SOYMON022 g3257794 BLASTX 217 1e−23 60 5723 9138 701119543H1 SOYMON037 g3257794 BLASTX 152 1e−13 58 5724 -700669394 700669394H1 SOYMON006 g1778518 BLASTX 75 1e−9 50 5725 3196 700753821H1 SOYMON014 g1778518 BLASTX 117 1e−9 59 5726 -700999272 700999272H1 SOYMON018 g1326254 BLASTX 153 1e−15 57 5727 32509 LIB3055-011- LIB3055 g1778518 BLASTX 124 1e−27 35 Q1-N1-G1 MAIZE ALANINE AMINOTRANSFERASE 5728 -700049393 700049393H1 SATMON003 g296204 BLASTX 143 1e−12 100 5729 -700104304 700104304H1 SATMON010 g1353351 BLASTN 655 1e−45 70 5730 -700172189 700172189H1 SATMON013 g1353352 BLASTX 211 1e−22 70 5731 -700222553 700222553H1 SATMON011 g1353352 BLASTX 292 1e−33 54 5732 -700257069 700257069H1 SATMON017 g469147 BLASTN 610 1e−42 70 5733 -700264090 700264090H1 SATMON017 g296203 BLASTN 798 1e−57 77 5734 -700264413 700264413H1 SATMON017 g296204 BLASTX 319 1e−37 59 5735 -700457290 700457290H1 SATMON029 g296203 BLASTN 640 1e−44 70 5736 -700461128 700461128H1 SATMON033 g469147 BLASTN 482 1e−31 65 5737 -700461228 700461228H1 SATMON033 g296204 BLASTX 120 1e−19 61 5738 -700579019 700579019H1 SATMON031 g1353352 BLASTX 149 1e−16 39 5739 -700584206 700584206H1 SATMON031 g1353352 BLASTX 175 1e−17 62 5740 -700617436 700617436H1 SATMON033 g296204 BLASTX 206 1e−24 51 5741 -700624223 700624223H1 SATMON034 g1353351 BLASTN 476 1e−29 72 5742 -701164032 701164032H1 SATMONN04 g296204 BLASTX 85 1e−11 65 5743 -701166826 701166826H1 SATMONN04 g296203 BLASTN 219 1e−12 84 5744 15087 700801716H1 SATMON036 g296203 BLASTN 434 1e−25 91 5745 15087 700806781H1 SATMON036 g469147 BLASTN 198 1e−11 87 5746 15418 700102926H1 SATMON010 g1353351 BLASTN 550 1e−35 65 5747 15418 700423101H1 SATMONN01 g1353351 BLASTN 475 1e−29 66 5748 22920 701172883H2 SATMONN05 g469147 BLASTN 778 1e−56 77 5749 22920 701172884H2 SATMONN05 g469147 BLASTN 460 1e−51 77 5750 2698 700099203H1 SATMON009 g1353352 BLASTX 192 1e−18 82 5751 29667 700210632H1 SATMON016 g1353352 BLASTX 260 1e−28 57 5752 31650 700580511H1 SATMON031 g1353352 BLASTX 192 1e−35 68 5753 3823 700217635H1 SATMON016 g296203 BLASTN 650 1e−45 76 5754 3823 700349242H1 SATMON023 g296203 BLASTN 524 1e−34 76 5755 414 700473110H1 SATMON025 g296204 BLASTX 204 1e−35 57 5756 414 700264510H1 SATMON017 g469147 BLASTN 456 1e−27 60 5757 414 700262355H1 SATMON017 g469148 BLASTX 241 1e−26 55 5758 414 700263001H1 SATMON017 g469148 BLASTX 230 1e−24 56 5759 414 700474691H1 SATMON025 g296204 BLASTX 179 1e−17 44 5760 414 700615134H1 SATMON033 g469148 BLASTX 127 1e−10 62 5761 6080 700218182H1 SATMON016 g296203 BLASTN 684 1e−48 74 5762 6080 700239054H1 SATMON010 g296203 BLASTN 649 1e−45 74 5763 6080 700207743H1 SATMON016 g296203 BLASTN 592 1e−40 74 5764 6080 700049234H1 SATMON003 g296204 BLASTX 144 1e−12 64 5765 8847 700257223H1 SATMON017 g296204 BLASTX 218 1e−23 54 5766 8847 700267629H1 SATMON017 g296204 BLASTX 184 1e−18 50 5767 8847 700267912H1 SATMON017 g296204 BLASTX 184 1e−18 50 5768 8847 700265819H1 SATMON017 g296204 BLASTX 136 1e−11 43 5769 923 700047471H1 SATMON003 g296203 BLASTN 1211 1e−103 92 5770 923 700446631H1 SATMON027 g296203 BLASTN 766 1e−102 92 5771 923 700263484H1 SATMON017 g296203 BLASTN 1332 1e−102 94 5772 923 700076095H1 SATMON007 g296203 BLASTN 1284 1e−98 93 5773 923 700042264H1 SATMON004 g296203 BLASTN 1267 1e−96 93 5774 923 700041605H1 SATMON004 g296203 BLASTN 1245 1e−94 92 5775 923 700258238H1 SATMON017 g296203 BLASTN 933 1e−93 89 5776 923 700620967H1 SATMON034 g296203 BLASTN 1011 1e−92 91 5777 923 700046079H1 SATMON004 g296203 BLASTN 1211 1e−92 94 5778 923 700073909H1 SATMON007 g296203 BLASTN 1203 1e−91 91 5779 923 701179662H1 SATMONN05 g296203 BLASTN 1194 1e−90 93 5780 923 700045425H1 SATMON004 g296203 BLASTN 1196 1e−90 92 5781 923 700043325H1 SATMON004 g296203 BLASTN 1178 1e−89 93 5782 923 700042080H1 SATMON004 g296203 BLASTN 1061 1e−86 92 5783 923 700799695H1 SATMON036 g296203 BLASTN 1139 1e−86 92 5784 923 700347121H1 SATMON021 g296203 BLASTN 1017 1e−85 88 5785 923 700194649H1 SATMON014 g296203 BLASTN 1129 1e−85 91 5786 923 700803015H1 SATMON036 g296203 BLASTN 959 1e−84 91 5787 923 700046202H1 SATMON004 g296203 BLASTN 1118 1e−84 94 5788 923 700621382H1 SATMON034 g296203 BLASTN 648 1e−83 92 5789 923 700194809H1 SATMON014 g296203 BLASTN 1083 1e−81 94 5790 923 700194576H1 SATMON014 g296203 BLASTN 1089 1e−81 92 5791 923 700045006H1 SATMON004 g296203 BLASTN 1076 1e−80 91 5792 923 700195835H1 SATMON014 g296203 BLASTN 1057 1e−79 91 5793 923 700194814H1 SATMON014 g296203 BLASTN 1058 1e−79 92 5794 923 700046245H1 SATMON004 g296203 BLASTN 1046 1e−78 94 5795 923 700161109H1 SATMON012 g296203 BLASTN 1047 1e−78 94 5796 923 700194345H1 SATMON014 g296203 BLASTN 1037 1e−77 94 5797 923 700472892H1 SATMON025 g296203 BLASTN 505 1e−76 88 5798 923 700617757H1 SATMON033 g296203 BLASTN 863 1e−76 90 5799 923 700805426H1 SATMON036 g296203 BLASTN 523 1e−74 93 5800 923 700801191H1 SATMON036 g296203 BLASTN 724 1e−74 90 5801 923 700472860H1 SATMON025 g296203 BLASTN 876 1e−74 86 5802 923 700100107H1 SATMON009 g296203 BLASTN 999 1e−74 88 5803 923 700465264H1 SATMON025 g296203 BLASTN 784 1e−72 92 5804 923 700455079H1 SATMON029 g296203 BLASTN 930 1e−72 89 5805 923 700620492H1 SATMON034 g296203 BLASTN 718 1e−71 92 5806 923 700801419H1 SATMON036 g296203 BLASTN 909 1e−71 92 5807 923 700155082H1 SATMON007 g296203 BLASTN 949 1e−70 93 5808 923 700045844H1 SATMON004 g296203 BLASTN 808 1e−69 90 5809 923 700477823H1 SATMON025 g296203 BLASTN 922 1e−68 88 5810 923 700475452H1 SATMON025 g296203 BLASTN 824 1e−65 91 5811 923 700802280H1 SATMON036 g296203 BLASTN 874 1e−64 92 5812 923 700156653H1 SATMON012 g296203 BLASTN 780 1e−63 87 5813 923 700444754H1 SATMON027 g296203 BLASTN 831 1e−60 89 5814 923 700099483H1 SATMON009 g296203 BLASTN 724 1e−59 88 5815 923 700101871H1 SATMON009 g296203 BLASTN 821 1e−59 91 5816 923 700076559H1 SATMON007 g296203 BLASTN 765 1e−57 89 5817 923 700442606H1 SATMON026 g296203 BLASTN 791 1e−57 91 5818 923 700800871H1 SATMON036 g296203 BLASTN 494 1e−56 86 5819 923 700197582H1 SATMON014 g296203 BLASTN 786 1e−56 90 5820 923 700100451H1 SATMON009 g296203 BLASTN 476 1e−54 90 5821 923 700405018H1 SATMON027 g296203 BLASTN 597 1e−54 86 5822 923 700099885H1 SATMON009 g296203 BLASTN 653 1e−53 91 5823 923 700043273H1 SATMON004 g296203 BLASTN 721 1e−51 90 5824 923 700476434H1 SATMON025 g296203 BLASTN 449 1e−47 91 5825 923 700438820H1 SATMON026 g296203 BLASTN 671 1e−47 89 5826 923 700428681H1 SATMONN01 g296203 BLASTN 673 1e−47 91 5827 923 700042259H1 SATMON004 g296203 BLASTN 675 1e−47 93 5828 923 700801436H1 SATMON036 g296203 BLASTN 677 1e−47 86 5829 923 700257814H1 SATMON017 g296203 BLASTN 647 1e−45 85 5830 923 700044879H1 SATMON004 g296203 BLASTN 648 1e−45 91 5831 923 700207027H1 SATMON003 g296203 BLASTN 595 1e−42 87 5832 923 700257265H1 SATMON017 g296203 BLASTN 610 1e−42 87 5833 923 700571949H1 SATMON030 g296203 BLASTN 576 1e−39 91 5834 923 701166609H1 SATMONN04 g296203 BLASTN 514 1e−38 83 5835 923 701182932H1 SATMONN06 g296203 BLASTN 383 1e−37 88 5836 923 700281788H1 SATMON020 g296203 BLASTN 398 1e−37 88 5837 923 700151478H1 SATMON007 g296203 BLASTN 554 1e−37 89 5838 923 700423955H1 SATMONN01 g296203 BLASTN 539 1e−36 85 5839 923 700472592H1 SATMON025 g296203 BLASTN 291 1e−34 87 5840 923 700621067H2 SATMON034 g296203 BLASTN 480 1e−31 84 5841 923 700621082H2 SATMON034 g296203 BLASTN 457 1e−29 90 5842 923 700426976H1 SATMONN01 g296203 BLASTN 431 1e−27 93 5843 923 700098538H1 SATMON009 g296204 BLASTX 117 1e−9 69 5844 9316 700263427H1 SATMON017 g1353352 BLASTX 318 1e−36 63 5845 9316 700222070H1 SATMON011 g1353352 BLASTX 296 1e−33 61 5846 9316 700085696H1 SATMON011 g1353352 BLASTX 259 1e−28 67 5847 -L30601398 LIB3060-001- LIB3060 g296203 BLASTN 610 1e−67 88 Q1-K2-F11 5848 -L30603921 LIB3060-042- LIB3060 g296203 BLASTN 740 1e−63 83 Q1-K1-E6 5849 -L30672268 LIB3067-007- LIB3067 g296203 BLASTN 601 1e−41 85 Q1-K1-H12 5850 -L30695453 LIB3069-036- LIB3069 g296203 BLASTN 868 1e−63 75 Q1-K1-C10 5851 -L832403 LIB83-005- LIB83 g469148 BLASTX 210 1e−37 81 Q1-E1-A7 5852 29667 LIB3060-015- LIB3060 g1353351 BLASTN 631 1e−42 61 Q1-K1-B3 5853 31650 LIB148-034- LIB148 g1353352 BLASTX 127 1e−53 63 Q1-E1-A6 5854 923 LIB3067-040- LIB3067 g296203 BLASTN 1949 1e−153 94 Q1-K1-B11 5855 923 LIB3060-017- LIB3060 g296203 BLASTN 1832 1e−143 92 Q1-K1-F12 5856 923 LIB143-053- LIB143 g296203 BLASTN 1814 1e−142 91 Q1-E1-G9 5857 923 LIB148-002- LIB148 g296203 BLASTN 1821 1e−142 94 Q1-E1-B9 5858 923 LIB36-012- LIB36 g296203 BLASTN 1766 1e−140 92 Q1-E1-B11 5859 923 LIB84-004- LIB84 g296203 BLASTN 1797 1e−140 91 Q1-E1-F6 5860 923 LIB3066-019- LIB3066 g296203 BLASTN 1520 1e−139 94 Q1-K1-E9 5861 923 LIB3059-045- LIB3059 g296203 BLASTN 1777 1e−139 92 Q1-K1-G1 5862 923 LIB3059-014- LIB3059 g296203 BLASTN 1785 1e−139 91 Q1-K1-H7 5863 923 LIB3060-044- LIB3060 g296203 BLASTN 1007 1e−136 92 Q1-K1-E2 5864 923 LIB3060-012- LIB3060 g296203 BLASTN 1662 1e−134 91 Q1-K1-C8 5865 923 LIB189-019- LIB189 g296203 BLASTN 1642 1e−131 92 Q1-E1-D11 5866 923 LIB3059-014- LIB305 g296203 BLASTN 1232 1e−129 88 Q1-K1-A8 5867 923 LIB143-053- LIB143 g296203 BLASTN 1377 1e−129 90 Q1-E1-G10 5868 923 LIB3059-006- LIB3059 g296203 BLASTN 1532 1e−124 88 Q1-K1-H5 5869 923 LIB3060-023- LIB3060 g296203 BLASTN 1176 1e−122 85 Q1-K1-E6 5870 923 LIB36-017- LIB36 g296203 BLASTN 1545 1e−119 91 Q1-E1-D3 5871 923 LIB3060-023- LIB3060 g296203 BLASTN 1418 1e−109 79 Q1-K1-E7 5872 923 LIB3060-036- LIB3060 g296203 BLASTN 1410 1e−108 92 Q1-K1-D2 5873 923 LIB3060-002- LIB3060 g296203 BLASTN 1400 1e−107 91 Q1-K2-C11 5874 923 LIB36-013- LIB36 g296203 BLASTN 1202 1e−100 87 Q1-E1-C3 5875 923 LIB3079-021- LIB3079 g296203 BLASTN 1236 1e−100 90 Q1-K1-D8 5876 923 LIB3060-051- LIB3060 g296203 BLASTN 1281 1e−97 88 Q1-K1-B8 5877 923 LIB3059-048- LIB3059 g296203 BLASTN 1224 1e−93 94 Q1-K1-A4 5878 923 LIB3060-043- LIB3060 g296203 BLASTN 816 1e−90 92 Q1-K1-G9 5879 923 LIB3060-034- LIB3060 g296203 BLASTN 816 1e−87 88 Q1-K1-A5 5880 923 LIB3060-042- LIB3060 g296203 BLASTN 1126 1e−85 91 Q1-K1-E4 5881 923 LIB3060-011- LIB3060 g296203 BLASTN 790 1e−78 86 Q1-K1-A9 5882 923 LIB189-033- LIB189 g296203 BLASTN 566 1e−74 83 Q1-E1-F2 5883 923 LIB3061-041- LIB3061 g296203 BLASTN 809 1e−68 89 Q1-K1-B2 5884 923 LIB3060-030- LIB3060 g296203 BLASTN 472 1e−65 73 Q1-K1-E1 5885 923 LIB3060-004- LIB3060 g296203 BLASTN 407 1e−38 78 Q1-K1-A8 5886 9316 LIB3062-014- LIB3062 g1353352 BLASTX 448 1e−71 60 Q1-K1-A12 5887 9316 LIB3060-041- LIB3060 g1353352 BLASTX 393 1e−68 58 Q1-K1-C8 5888 9316 LIB84-028- LIB84 g1353352 BLASTX 202 1e−61 61 Q1-E1-H9 SOYBEAN ALANINE AMINOTRANSFERASE 5889 -700743719 700743719H1 SOYMON012 g1353352 BLASTX 78 1e−8 61 5890 -700959696 700959696H1 SOYMON022 g296204 BLASTX 195 1e−20 79 5891 -700996510 700996510H1 SOYMON018 g296204 BLASTX 187 1e−18 71 5892 -701069323 701069323H1 SOYMON034 g296204 BLASTX 116 1e−21 63 5893 10017 700605618H2 SOYMON005 g296203 BLASTN 496 1e−32 73 5894 10017 700682253H1 SOYMON008 g296204 BLASTX 143 1e−16 71 5895 10017 700990421H1 SOYMON011 g296204 BLASTX 160 1e−15 69 5896 10017 700747761H1 SOYMON013 g296204 BLASTX 164 1e−15 70 5897 10017 701038703H1 SOYMON029 g296204 BLASTX 164 1e−15 70 5898 10017 700975277H1 SOYMON009 g296204 BLASTX 140 1e−14 67 5899 10017 700984821H1 SOYMON009 g296204 BLASTX 155 1e−14 69 5900 10017 700756842H1 SOYMON014 g296204 BLASTX 139 1e−12 68 5901 10017 700746942H1 SOYMON013 g469147 BLASTN 241 1e−9 76 5902 10118 701120663H1 SOYMON037 g296204 BLASTX 350 1e−41 85 5903 10118 701049525H1 SOYMON032 g296204 BLASTX 355 1e−41 88 5904 10118 701119423H1 SOYMON037 g296203 BLASTN 575 1e−39 67 5905 10118 700872879H1 SOYMON018 g296204 BLASTX 312 1e−35 82 5906 10118 700973420H1 SOYMON005 g296204 BLASTX 260 1e−31 66 5907 12859 700562950H1 SOYMON002 g296203 BLASTN 685 1e−48 74 5908 12859 700971319H1 SOYMON005 g296204 BLASTX 273 1e−38 76 5909 17267 700555074H1 SOYMON001 g1353352 BLASTX 378 1e−45 79 5910 17267 700555060H1 SOYMON001 g1353352 BLASTX 378 1e−45 79 5911 17267 700743751H1 SOYMON012 g1353352 BLASTX 133 1e−11 61 5912 19812 700896952H1 SOYMON027 g296203 BLASTN 468 1e−30 67 5913 19812 700659743H1 SOYMON004 g296203 BLASTN 451 1e−27 67 5914 31650 700874484H1 SOYMON018 g1353352 BLASTX 118 1e−9 59 5915 5883 701001504H1 SOYMON018 g296203 BLASTN 714 1e−50 73 5916 5883 700969537H1 SOYMON005 g296203 BLASTN 598 1e−41 70 5917 5883 700672092H1 SOYMON006 g296203 BLASTN 601 1e−41 72 5918 5883 700961520H1 SOYMON022 g296203 BLASTN 584 1e−39 72 5919 5883 701141195H1 SOYMON038 g296204 BLASTX 153 1e−14 75 5920 6292 700559647H1 SOYMON001 g1353352 BLASTX 292 1e−33 51 5921 6292 700556715H1 SOYMON001 g1353352 BLASTX 292 1e−33 53 5922 6292 701001051H1 SOYMON018 g1353352 BLASTX 293 1e−33 58 5923 6292 700682468H2 SOYMON008 g1353352 BLASTX 261 1e−29 51 5924 6292 700973534H1 SOYMON005 g1353352 BLASTX 263 1e−29 54 5925 6292 700874672H1 SOYMON018 g1353352 BLASTX 150 1e−28 55 5926 6292 700893193H1 SOYMON024 g296204 BLASTX 256 1e−28 58 5927 6292 700681610H1 SOYMON008 g296204 BLASTX 259 1e−28 58 5928 6292 701002246H1 SOYMON018 g296204 BLASTX 159 1e−27 56 5929 6292 700956467H1 SOYMON022 g1353352 BLASTX 238 1e−27 58 5930 6292 700888645H1 SOYMON024 g296204 BLASTX 196 1e−20 60 5931 6292 701002201H1 SOYMON018 g296204 BLASTX 156 1e−16 57 5932 6292 700680675H1 SOYMON008 g469148 BLASTX 119 1e−9 63 5933 6292 701050803H1 SOYMON032 g296204 BLASTX 120 1e−9 58 5934 6594 700684722H1 SOYMON008 g1353352 BLASTX 157 1e−22 69 5935 6594 700872191H1 SOYMON018 g1353352 BLASTX 129 1e−16 61 5936 698 700738627H1 SOYMON012 g1353352 BLASTX 333 1e−39 73 5937 698 700681703H1 SOYMON008 g1353352 BLASTX 319 1e−37 76 5938 698 700961778H1 SOYMON022 g1353352 BLASTX 316 1e−36 79 5939 698 700666316H1 SOYMON005 g1353352 BLASTX 298 1e−34 77 5940 698 700685706H1 SOYMON008 g1353352 BLASTX 293 1e−33 72 5941 698 700739093H1 SOYMON012 g1353352 BLASTX 172 1e−29 73 5942 698 700666387H1 SOYMON005 g1353352 BLASTX 267 1e−29 76 5943 698 700993520H1 SOYMON011 g1353352 BLASTX 255 1e−28 63 5944 698 700896371H1 SOYMON027 g1353352 BLASTX 255 1e−28 80 5945 698 700997253H1 SOYMON018 g1353352 BLASTX 260 1e−28 65 5946 698 700995571H1 SOYMON011 g1353352 BLASTX 260 1e−28 63 5947 698 700648011H1 SOYMON003 g1353352 BLASTX 239 1e−25 66 5948 698 700850732H1 SOYMON023 g1353352 BLASTX 204 1e−21 78 5949 698 700557773H1 SOYMON001 g1353352 BLASTX 208 1e−21 81 5950 698 700874138H1 SOYMON018 g1353352 BLASTX 208 1e−21 81 5951 698 700559725H1 SOYMON001 g1353352 BLASTX 201 1e−20 82 5952 698 701105639H1 SOYMON036 g1353352 BLASTX 202 1e−20 80 5953 698 700994494H1 SOYMON011 g1353352 BLASTX 186 1e−18 83 5954 698 700738237H1 SOYMON012 g1353352 BLASTX 186 1e−18 78 5955 698 700555071H1 SOYMON001 g1353352 BLASTX 186 1e−18 83 5956 698 700786177H2 SOYMON011 g1353352 BLASTX 171 1e−17 54 5957 698 700554414H1 SOYMON001 g1353352 BLASTX 176 1e−17 84 5958 698 700741128H1 SOYMON012 g1353352 BLASTX 176 1e−17 82 5959 698 700965158H1 SOYMON022 g1353352 BLASTX 176 1e−17 82 5960 698 700685250H1 SOYMON008 g1353352 BLASTX 179 1e−17 80 5961 698 700991457H1 SOYMON011 g1353352 BLASTX 180 1e−17 82 5962 698 700684192H1 SOYMON008 g1353352 BLASTX 180 1e−17 82 5963 698 700871122H1 SOYMON018 g1353352 BLASTX 180 1e−17 82 5964 698 700997304H1 SOYMON018 g1353352 BLASTX 182 1e−17 70 5965 698 700685731H1 SOYMON008 g1353352 BLASTX 172 1e−16 82 5966 698 700685724H1 SOYMON008 g1353352 BLASTX 172 1e−16 82 5967 698 700739069H1 SOYMON012 g1353352 BLASTX 161 1e−15 83 5968 698 700741337H1 SOYMON012 g1353352 BLASTX 164 1e−15 81 5969 698 700683155H1 SOYMON008 g1353352 BLASTX 164 1e−15 81 5970 698 700994202H1 SOYMON011 g1353352 BLASTX 165 1e−15 73 5971 698 700555575H1 SOYMON001 g1353352 BLASTX 166 1e−15 79 5972 698 701000739H1 SOYMON018 g1353352 BLASTX 167 1e−15 63 5973 698 700740011H1 SOYMON012 g1353352 BLASTX 153 1e−14 83 5974 698 700994043H1 SOYMON011 g1353352 BLASTX 157 1e−14 81 5975 698 700555709H1 SOYMON001 g1353352 BLASTX 87 1e−12 76 5976 698 701107588H1 SOYMON036 g1353352 BLASTX 114 1e−12 68 5977 698 700871057H1 SOYMON018 g1353352 BLASTX 139 1e−12 77 5978 698 700744973H1 SOYMON013 g1353352 BLASTX 141 1e−12 79 5979 698 700741744H1 SOYMON012 g1353352 BLASTX 141 1e−12 79 5980 698 700792044H1 SOYMON011 g1353352 BLASTX 142 1e−12 63 5981 698 700993716H1 SOYMON011 g1353352 BLASTX 83 1e−11 83 5982 698 700684326H1 SOYMON008 g1353352 BLASTX 137 1e−11 81 5983 698 700989256H1 SOYMON011 g1353352 BLASTX 124 1e−10 77 5984 698 700791590H1 SOYMON011 g1353352 BLASTX 130 1e−10 78 5985 698 700872519H1 SOYMON018 g1353352 BLASTX 78 1e−9 78 5986 698 700645949H1 SOYMON011 g1353352 BLASTX 106 1e−9 63 5987 698 700996252H1 SOYMON018 g1353352 BLASTX 125 1e−9 77 5988 698 700876656H1 SOYMON018 g1353352 BLASTX 74 1e−8 79 5989 698 700874318H1 SOYMON018 g1353352 BLASTX 113 1e−8 73 5990 698 700737927H1 SOYMON012 g1353352 BLASTX 114 1e−8 73 5991 9687 700740448H1 SOYMON012 g1353352 BLASTX 262 1e−29 57 5992 9687 700954623H1 SOYMON022 g1353352 BLASTX 265 1e−29 56 5993 9687 701142577H1 SOYMON038 g1353352 BLASTX 247 1e−27 56 5994 9687 701000510H1 SOYMON018 g1353352 BLASTX 235 1e−25 65 5995 9687 700874683H1 SOYMON018 g1353352 BLASTX 212 1e−22 58 5996 9687 700874576H1 SOYMON018 g1353352 BLASTX 117 1e−17 54 5997 9687 700999910H1 SOYMON018 g1353352 BLASTX 163 1e−15 54 5998 9687 701001711H1 SOYMON018 g1353352 BLASTX 116 1e−8 64 5999 10017 LIB3030-005- LIB3030 g296204 BLASTX 159 1e−38 72 Q1-B1-F1 6000 10017 LIB3051-078- LIB3051 g296204 BLASTX 207 1e−37 61 Q1-K1-B5 6001 10017 LIB3051-006- LIB3051 g296203 BLASTN 543 1e−34 68 Q1-K1-D5 6002 10017 LIB3051-006- LIB3051 g469147 BLASTN 306 1e−14 69 Q1-E1-D5 6003 10017 LIB3051-113- LIB3051 g469147 BLASTN 301 1e−13 63 Q1-K1-B4 6004 698 LIB3028-005- LIB3028 g1353352 BLASTX 110 1e−34 69 Q1-B1-A11 MAIZE NADP-DEPENDENT MALIC ENZYME 6005 -700041501 700041501H1 SATMON004 g168527 BLASTN 529 1e−35 93 6006 -700051224 700051224H1 SATMON003 g20468 BLASTN 514 1e−32 81 6007 -700073375 700073375H1 SATMON007 g168527 BLASTN 584 1e−58 77 6008 -700101813 700101813H1 SATMON009 g168527 BLASTN 920 1e−88 100 6009 -700104958 700104958H1 SATMON010 g168527 BLASTN 363 1e−19 92 6010 -700219021 700219021H1 SATMON011 g1785859 BLASTN 467 1e−28 80 6011 -700346164 700346164H1 SATMON021 g510876 BLASTX 102 1e−18 78 6012 -700453338 700453338H1 SATMON028 g20468 BLASTN 716 1e−50 79 6013 -700460886 700460886H1 SATMON031 g168527 BLASTN 191 1e−14 92 6014 -700573176 700573176H1 SATMON030 g168527 BLASTN 277 1e−25 80 6015 -701182650 701182650H1 SATMONN06 g169326 BLASTN 572 1e−51 79 6016 10304 700349609H1 SATMON023 g20468 BLASTN 939 1e−69 81 6017 10304 700050528H1 SATMON003 g20468 BLASTN 945 1e−69 80 6018 10304 700242979H1 SATMON010 g20468 BLASTN 926 1e−68 82 6019 10304 700577075H1 SATMON031 g20468 BLASTN 919 1e−67 81 6020 10304 700381724H1 SATMON023 g20468 BLASTN 507 1e−59 76 6021 18769 700050667H1 SATMON003 g20468 BLASTN 452 1e−29 76 6022 18769 700076676H1 SATMON007 g20469 BLASTX 181 1e−18 77 6023 18769 700155440H1 SATMON007 g20469 BLASTX 140 1e−12 73 6024 2190 700071978H1 SATMON007 g425803 BLASTN 1045 1e−80 83 6025 2190 700202802H1 SATMON003 g425803 BLASTN 440 1e−79 81 6026 2190 700104846H1 SATMON010 g425803 BLASTN 537 1e−73 83 6027 2190 700444338H1 SATMON027 g425803 BLASTN 677 1e−65 84 6028 2190 700457069H1 SATMON029 g425803 BLASTN 428 1e−56 81 6029 2190 700457021H1 SATMON029 g425803 BLASTN 753 1e−56 83 6030 2190 701181152H1 SATMONN06 g1785859 BLASTN 577 1e−54 78 6031 2190 700445983H1 SATMON027 g1785859 BLASTN 607 1e−52 74 6032 2190 700142607H2 SATMON013 g1785859 BLASTN 684 1e−48 78 6033 412 700097657H1 SATMON009 g168527 BLASTN 1648 1e−128 99 6034 412 700098574H1 SATMON009 g168527 BLASTN 1605 1e−124 99 6035 412 700099850H1 SATMON009 g168527 BLASTN 1537 1e−119 97 6036 412 700097455H1 SATMON009 g168527 BLASTN 1527 1e−118 99 6037 412 700097222H1 SATMON009 g168527 BLASTN 1530 1e−118 98 6038 412 700097391H1 SATMON009 g168527 BLASTN 1520 1e−117 98 6039 412 700097849H1 SATMON009 g168527 BLASTN 1504 1e−116 99 6040 412 700101666H1 SATMON009 g168527 BLASTN 1495 1e−115 100 6041 412 700099890H1 SATMON009 g168527 BLASTN 1468 1e−113 98 6042 412 700097237H1 SATMON009 g168527 BLASTN 1313 1e−112 98 6043 412 700101278H1 SATMON009 g168527 BLASTN 1441 1e−111 99 6044 412 700101431H1 SATMON009 g168527 BLASTN 1450 1e−111 100 6045 412 700100860H1 SATMON009 g168527 BLASTN 1431 1e−110 99 6046 412 700581218H1 SATMON031 g168527 BLASTN 1403 1e−108 98 6047 412 700101446H1 SATMON009 g168527 BLASTN 1407 1e−108 99 6048 412 700044315H1 SATMON004 g168527 BLASTN 1390 1e−106 100 6049 412 700045610H1 SATMON004 g168527 BLASTN 1301 1e−105 98 6050 412 700434125H1 SATMONN01 g168527 BLASTN 1374 1e−105 97 6051 412 700041705H1 SATMON004 g168527 BLASTN 1311 1e−104 99 6052 412 700104088H1 SATMON010 g168527 BLASTN 1361 1e−104 92 6053 412 700614919H1 SATMON033 g168527 BLASTN 1103 1e−103 86 6054 412 700613108H1 SATMON033 g168527 BLASTN 1345 1e−103 89 6055 412 700042025H1 SATMON004 g168527 BLASTN 1352 1e−103 99 6056 412 700467944H1 SATMON025 g168527 BLASTN 1353 1e−103 95 6057 412 700617354H1 SATMON033 g168527 BLASTN 1354 1e−103 89 6058 412 700095156H1 SATMON008 g168527 BLASTN 1354 1e−103 92 6059 412 700448457H1 SATMON027 g168527 BLASTN 722 1e−102 93 6060 412 700581224H1 SATMON031 g168527 BLASTN 872 1e−101 98 6061 412 700426724H1 SATMONN01 g168527 BLASTN 1322 1e−101 98 6062 412 700105096H1 SATMON010 g168527 BLASTN 707 1e−100 93 6063 412 700045272H1 SATMON004 g168527 BLASTN 1311 1e−100 99 6064 412 700577375H1 SATMON031 g168527 BLASTN 1300 1e−99 100 6065 412 700044113H1 SATMON004 g168527 BLASTN 1300 1e−99 100 6066 412 700042068H1 SATMON004 g168527 BLASTN 1301 1e−99 99 6067 412 700582457H1 SATMON031 g168527 BLASTN 1305 1e−99 98 6068 412 700580693H1 SATMON031 g168527 BLASTN 975 1e−98 97 6069 412 700577922H1 SATMON031 g168527 BLASTN 1111 1e−98 95 6070 412 700043222H1 SATMON004 g168527 BLASTN 1289 1e−98 99 6071 412 700103882H1 SATMON010 g168527 BLASTN 1277 1e−97 92 6072 412 700579779H1 SATMON031 g168527 BLASTN 1282 1e−97 98 6073 412 700615410H1 SATMON033 g168527 BLASTN 829 1e−96 91 6074 412 700439978H1 SATMON026 g168527 BLASTN 1264 1e−96 99 6075 412 700045066H1 SATMON004 g168527 BLASTN 1268 1e−96 98 6076 412 700439024H1 SATMON026 g168527 BLASTN 1041 1e−95 96 6077 412 700263465H1 SATMON017 g168527 BLASTN 1088 1e−94 90 6078 412 700046417H1 SATMON004 g168527 BLASTN 1240 1e−94 100 6079 412 700347845H1 SATMON023 g168527 BLASTN 1241 1e−94 92 6080 412 700043227H1 SATMON004 g168527 BLASTN 1241 1e−94 97 6081 412 700469957H1 SATMON025 g168527 BLASTN 1243 1e−94 95 6082 412 700044725H1 SATMON004 g168527 BLASTN 1246 1e−94 99 6083 412 700615834H1 SATMON033 g168527 BLASTN 777 1e−93 93 6084 412 700224349H1 SATMON011 g168527 BLASTN 1230 1e−93 92 6085 412 700438840H1 SATMON026 g168527 BLASTN 675 1e−92 100 6086 412 700465188H1 SATMON025 g168527 BLASTN 1133 1e−92 91 6087 412 700223493H1 SATMON011 g168527 BLASTN 1222 1e−92 94 6088 412 700442430H1 SATMON026 g168527 BLASTN 490 1e−91 95 6089 412 700479665H1 SATMON034 g168527 BLASTN 1199 1e−91 93 6090 412 700242318H1 SATMON010 g168527 BLASTN 1200 1e−91 96 6091 412 700262339H1 SATMON017 g168527 BLASTN 924 1e−90 91 6092 412 700551426H1 SATMON022 g168527 BLASTN 1197 1e−90 93 6093 412 700580501H1 SATMON031 g168527 BLASTN 674 1e−89 91 6094 412 700430624H1 SATMONN01 g168527 BLASTN 839 1e−89 96 6095 412 700798989H1 SATMON036 g168527 BLASTN 1176 1e−89 90 6096 412 700438471H1 SATMON026 g168527 BLASTN 1183 1e−89 96 6097 412 700572903H1 SATMON030 g168527 BLASTN 771 1e−88 89 6098 412 700083411H1 SATMON011 g168527 BLASTN 1096 1e−88 92 6099 412 700442605H1 SATMON026 g168527 BLASTN 1170 1e−88 88 6100 412 700224532H1 SATMON011 g168527 BLASTN 1170 1e−88 92 6101 412 700572585H1 SATMON030 g168527 BLASTN 912 1e−87 87 6102 412 700083289H1 SATMON011 g168527 BLASTN 1155 1e−87 90 6103 412 700612607H1 SATMON033 g168527 BLASTN 634 1e−86 91 6104 412 700429569H1 SATMONN01 g168527 BLASTN 1115 1e−84 90 6105 412 700048813H1 SATMON003 g168527 BLASTN 844 1e−83 89 6106 412 700422905H1 SATMONN01 g168527 BLASTN 872 1e−83 93 6107 412 700106553H1 SATMON010 g168527 BLASTN 888 1e−83 87 6108 412 700101622H1 SATMON009 g168527 BLASTN 1105 1e−83 100 6109 412 700168331H1 SATMON013 g168527 BLASTN 1108 1e−83 90 6110 412 701183573H1 SATMONN06 g168527 BLASTN 1098 1e−82 89 6111 412 700355825H1 SATMON024 g168527 BLASTN 1102 1e−82 88 6112 412 700171967H1 SATMON013 g168527 BLASTN 1085 1e−81 92 6113 412 700239492H1 SATMON010 g168527 BLASTN 1086 1e−81 91 6114 412 701160628H1 SATMONN04 g168527 BLASTN 624 1e−79 89 6115 412 700020733H1 SATMON001 g168527 BLASTN 1048 1e−78 92 6116 412 700575032H1 SATMON030 g168527 BLASTN 493 1e−77 91 6117 412 700241204H1 SATMON010 g168527 BLASTN 812 1e−77 88 6118 412 700447091H1 SATMON027 g168527 BLASTN 991 1e−77 91 6119 412 700469827H1 SATMON025 g168527 BLASTN 643 1e−76 87 6120 412 700043868H1 SATMON004 g168527 BLASTN 1020 1e−76 100 6121 412 700167416H1 SATMON013 g168527 BLASTN 1021 1e−76 92 6122 412 700166313H1 SATMON013 g168527 BLASTN 1010 1e−75 93 6123 412 700477627H1 SATMON025 g168527 BLASTN 1010 1e−75 88 6124 412 700043873H1 SATMON004 g168527 BLASTN 1015 1e−75 100 6125 412 700027363H1 SATMON003 g168527 BLASTN 402 1e−73 92 6126 412 700569811H1 SATMON030 g168527 BLASTN 593 1e−71 89 6127 412 700551661H1 SATMON022 g168527 BLASTN 860 1e−71 86 6128 412 700613723H1 SATMON033 g168527 BLASTN 962 1e−71 86 6129 412 700171193H1 SATMON013 g168527 BLASTN 935 1e−69 89 6130 412 700164679H1 SATMON013 g168527 BLASTN 924 1e−68 88 6131 412 700570921H1 SATMON030 g168527 BLASTN 455 1e−67 88 6132 412 701160615H1 SATMONN04 g168527 BLASTN 694 1e−67 84 6133 412 700154717H1 SATMON007 g168527 BLASTN 893 1e−65 90 6134 412 700475530H1 SATMON025 g168527 BLASTN 328 1e−63 90 6135 412 700203726H1 SATMON003 g168527 BLASTN 410 1e−63 91 6136 412 700241493H1 SATMON010 g168527 BLASTN 796 1e−63 89 6137 412 700438637H1 SATMON026 g168527 BLASTN 493 1e−62 96 6138 412 700100702H1 SATMON009 g168527 BLASTN 848 1e−61 98 6139 412 700223081H1 SATMON011 g168527 BLASTN 649 1e−56 89 6140 412 700099413H1 SATMON009 g168527 BLASTN 767 1e−55 83 6141 412 700613195H1 SATMON033 g168527 BLASTN 633 1e−53 83 6142 412 700158857H1 SATMON012 g168527 BLASTN 745 1e−53 89 6143 412 700439831H1 SATMON026 g168527 BLASTN 498 1e−50 95 6144 412 700017622H1 SATMON001 g168527 BLASTN 662 1e−46 89 6145 412 700224833H1 SATMON011 g168527 BLASTN 636 1e−44 89 6146 412 700099061H1 SATMON009 g168527 BLASTN 637 1e−44 95 6147 412 700577851H1 SATMON031 g168527 BLASTN 637 1e−44 95 6148 412 700100884H1 SATMON009 g168527 BLASTN 637 1e−44 95 6149 412 700466638H1 SATMON025 g168527 BLASTN 640 1e−44 85 6150 412 700614366H1 SATMON033 g415314 BLASTN 644 1e−44 88 6151 412 700084389H1 SATMON011 g168527 BLASTN 545 1e−43 90 6152 412 700090184H1 SATMON011 g168527 BLASTN 615 1e−42 100 6153 412 700099462H1 SATMON009 g168527 BLASTN 615 1e−42 100 6154 412 700098372H1 SATMON009 g168527 BLASTN 596 1e−40 99 6155 412 700432379H1 SATMONN01 g168527 BLASTN 341 1e−39 94 6156 412 700101636H1 SATMON009 g168527 BLASTN 524 1e−38 92 6157 412 700090392H1 SATMON011 g168527 BLASTN 532 1e−35 90 6158 412 700282016H1 SATMON022 g415314 BLASTN 534 1e−35 86 6159 412 700042404H1 SATMON004 g168527 BLASTN 525 1e−34 100 6160 412 700465190H1 SATMON025 g168527 BLASTN 509 1e−33 87 6161 412 700260024H1 SATMON017 g168527 BLASTN 210 1e−32 94 6162 412 700579166H1 SATMON031 g168527 BLASTN 413 1e−32 96 6163 412 700049441H1 SATMON003 g168527 BLASTN 303 1e−31 90 6164 412 700618285H1 SATMON033 g168527 BLASTN 454 1e−28 85 6165 412 700259602H1 SATMON017 g168527 BLASTN 297 1e−26 89 6166 412 700467465H1 SATMON025 g168527 BLASTN 420 1e−26 96 6167 412 700215437H1 SATMON016 g168527 BLASTN 306 1e−20 86 6168 412 700265281H1 SATMON017 g168527 BLASTN 359 1e−19 89 6169 6503 700083127H1 SATMON011 g168528 BLASTX 124 1e−10 92 6170 9238 700336628H1 SATMON019 g168527 BLASTN 435 1e−34 74 6171 9238 700017544H1 SATMON001 g168527 BLASTN 513 1e−33 74 6172 -L1485987 LIB148-042- LIB148 g415314 BLASTN 566 1e−38 76 Q1-E1-D11 6173 -L30602419 LIB3060-012- LIB3060 g168527 BLASTN 723 1e−51 96 Q1-K1-E8 6174 -L30611342 LIB3061-002- LIB3061 g168527 BLASTN 633 1e−43 77 Q1-K1-H10 6175 -L30662912 LIB3066-008- LIB3066 g2911148 BLASTX 147 1e−29 84 Q1-K1-A2 6176 -L30664918 LIB3066-021- LIB3066 g168527 BLASTN 838 1e−60 71 Q1-K1-B5 6177 -L30672727 LIB3067-039- LIB3067 g168527 BLASTN 401 1e−42 82 Q1-K1-C10 6178 -L30782241 LIB3078-007- LIB3078 g168527 BLASTN 393 1e−36 79 Q1-K1-A1 6179 -L30783451 LIB3078-050- LIB3078 g168527 BLASTN 199 1e−9 83 Q1-K1-G11 6180 -L30784158 LIB3078-035- LIB3078 g168527 BLASTN 201 1e−14 91 Q1-K1-H5 6181 30424 LIB3060-024- LIB3060 g415314 BLASTN 1355 1e−104 79 Q1-K1-D9 6182 412 LIB3078-022- LIB3078 g168527 BLASTN 2209 1e−175 95 Q1-K1-D10 6183 412 LIB3060-021- LIB3060 g168527 BLASTN 2203 1e−174 99 Q1-K1-G10 6184 412 LIB189-006- LIB189 g168527 BLASTN 2121 1e−167 99 Q1-E1-D2 6185 412 LIB189-010- LIB189 g168527 BLASTN 1749 1e−164 98 Q1-E1-C4 6186 412 LIB189-029- LIB189 g168527 BLASTN 2067 1e−163 98 Q1-E1-A5 6187 412 LIB36-021- LIB36 g168527 BLASTN 2011 1e−158 97 Q1-E1-D12 6188 412 LIB36-003- LIB36 g168527 BLASTN 1988 1e−156 95 Q1-E1-B4 6189 412 LIB36-017- LIB36 g168527 BLASTN 1503 1e−155 98 Q1-E1-D7 6190 412 LIB189-018- LIB189 g168527 BLASTN 1977 1e−155 97 Q1-E1-D11 6191 412 LIB189-014- LIB189 g168527 BLASTN 1941 1e−152 97 Q1-E1-D11 6192 412 LIB3078-049- LIB3078 g168527 BLASTN 1810 1e−151 94 Q1-K1-G10 6193 412 LIB3078-012- LIB3078 g168527 BLASTN 1874 1e−151 93 Q1-K1-E8 6194 412 LIB36-018- LIB36 g168527 BLASTN 1466 1e−150 97 Q1-E1-B9 6195 412 LIB36-012- LIB36 g168527 BLASTN 1901 1e−149 98 Q1-E1-H9 6196 412 LIB189-027- LIB189 g168527 BLASTN 1903 1e−149 95 Q1-E1-C5 6197 412 LIB84-005- LIB84 g168527 BLASTN 1889 1e−148 96 Q1-E1-A11 6198 412 LIB189-018- LIB189 g168527 BLASTN 1814 1e−144 97 Q1-E1-G7 6199 412 LIB3079-004- LIB3079 g168527 BLASTN 1724 1e−140 91 Q1-K1-A10 6200 412 LIB189-028- LIB189 g168527 BLASTN 1740 1e−140 99 Q1-E1-F11 6201 412 LIB84-029- LIB84 g168527 BLASTN 1795 1e−140 99 Q1-E1-A6 6202 412 LIB3060-002- LIB3060 g168527 BLASTN 1779 1e−139 95 Q1-K2-A8 6203 412 LIB3067-049- LIB3067 g168527 BLASTN 1098 1e−137 88 Q1-K1-F5 6204 412 LIB3062-026- LIB3062 g168527 BLASTN 1428 1e−135 89 Q1-K1-C8 6205 412 LIB3059-011- LIB3059 g168527 BLASTN 1651 1e−128 87 Q1-K1-C4 6206 412 LIB3061-002- LIB3061 g168527 BLASTN 1618 1e−125 89 Q1-K2-H10 6207 412 LIB3060-008- LIB3060 g168527 BLASTN 990 1e−122 97 Q1-K1-H3 6208 412 LIB3060-020- LIB3060 g168527 BLASTN 1322 1e−121 89 Q1-K1-E10 6209 412 LIB189-032- LIB189 g168527 BLASTN 680 1e−120 94 Q1-E1-E7 6210 412 LIB36-019- LIB36 g168527 BLASTN 1197 1e−115 97 Q1-E1-F11 6211 412 LIB3062-038- LIB3062 g168527 BLASTN 1498 1e−115 91 Q1-K1-D1 6212 412 LIB189-029- LIB189 g168527 BLASTN 1175 1e−113 95 Q1-E1-A4 6213 412 LIB36-022- LIB36 g168527 BLASTN 1393 1e−107 98 Q1-E1-F12 6214 412 LIB3079-001- LIB3079 g168527 BLASTN 1243 1e−103 82 Q1-K1-H3 6215 412 LIB189-014- LIB189 g168527 BLASTN 855 1e−99 91 Q1-E1-D12 6216 412 LIB189-026- LIB189 g168527 BLASTN 1167 1e−93 94 Q1-E1-C1 6217 412 LIB3079-001- LIB3079 g168527 BLASTN 480 1e−78 84 Q1-K1-H5 6218 412 LIB36-008- LIB36 g168527 BLASTN 576 1e−75 97 Q1-E1-C5 6219 412 LIB83-015- LIB83 g168527 BLASTN 446 1e−59 92 Q1-E1-G7 6220 412 LIB3062-024- LIB3062 g168527 BLASTN 455 1e−53 77 Q1-K1-D2 6221 412 LIB3062-026- LIB3062 g168527 BLASTN 561 1e−50 78 Q1-K1-C4 6222 412 LIB83-013- LIB83 g168527 BLASTN 637 1e−44 95 Q1-E1-E12 6223 412 LIB83-002- LIB83 g168527 BLASTN 564 1e−43 97 Q1-E1-F4 SOYBEAN NADP-DEPENDENT MALIC ENZYME 6224 -700698057 700698057H1 SOYMON015 g168527 BLASTN 513 1e−67 90 6225 -700744209 700744209H1 SOYMON013 g1679885 BLASTX 138 1e−12 69 6226 -700979875 700979875H2 SOYMON009 g20468 BLASTN 236 1e−8 82 6227 -701013601 701013601H1 SOYMON019 g20469 BLASTX 184 1e−18 60 6228 -701054477 701054477H1 SOYMON032 g169326 BLASTN 1122 1e−84 94 6229 -701206630 701206630H1 SOYMON035 g1679885 BLASTX 142 1e−14 85 6230 11537 700653458H1 SOYMON003 g20468 BLASTN 1173 1e−88 83 6231 11537 700650905H1 SOYMON003 g20468 BLASTN 886 1e−74 83 6232 11537 701141562H1 SOYMON038 g20468 BLASTN 532 1e−52 78 6233 11537 701144577H1 SOYMON031 g20468 BLASTN 624 1e−50 81 6234 11537 700748911H1 SOYMON013 g18460 BLASTX 91 1e−14 100 6235 11795 700667578H1 SOYMON006 g169326 BLASTN 1118 1e−84 95 6236 11795 701056334H1 SOYMON032 g169326 BLASTN 658 1e−82 94 6237 11795 700742616H1 SOYMON012 g169326 BLASTN 848 1e−61 95 6238 12499 701051365H1 SOYMON032 g169326 BLASTN 1237 1e−94 92 6239 12499 701102792H1 SOYMON028 g169326 BLASTN 1169 1e−88 92 6240 12499 701098731H2 SOYMON028 g169326 BLASTN 1031 1e−82 91 6241 15256 700744584H1 SOYMON013 g20469 BLASTX 96 1e−9 85 6242 1729 701000647H1 SOYMON018 g20468 BLASTN 766 1e−61 81 6243 1729 700738988H1 SOYMON012 g2150026 BLASTN 745 1e−53 85 6244 1729 700956234H1 SOYMON022 g20468 BLASTN 740 1e−52 74 6245 1729 700888666H1 SOYMON024 g2150026 BLASTN 626 1e−43 83 6246 1729 700752533H1 SOYMON014 g2150026 BLASTN 431 1e−34 80 6247 1729 700685485H1 SOYMON008 g459441 BLASTX 163 1e−15 82 6248 1729 700998862H1 SOYMON018 g20469 BLASTX 147 1e−14 73 6249 1729 700729313H1 SOYMON009 g2150029 BLASTX 85 1e−10 75 6250 17352 700846094H1 SOYMON021 g20468 BLASTN 700 1e−49 76 6251 17352 701062346H1 SOYMON033 g20468 BLASTN 658 1e−45 86 6252 17352 700866471H1 SOYMON016 g169326 BLASTN 511 1e−39 84 6253 21165 701129419H1 SOYMON037 g169326 BLASTN 1098 1e−85 92 6254 21165 701099310H1 SOYMON028 g169326 BLASTN 534 1e−54 87 6255 21165 701103522H1 SOYMON028 g169326 BLASTN 764 1e−54 92 6256 21165 701050730H1 SOYMON032 g169326 BLASTN 460 1e−43 88 6257 21165 701045037H1 SOYMON032 g169326 BLASTN 536 1e−43 89 6258 21165 701050806H1 SOYMON032 g169326 BLASTN 515 1e−41 89 6259 21165 700749793H1 SOYMON013 g169326 BLASTN 258 1e−40 86 6260 23648 701045082H1 SOYMON032 g169326 BLASTN 825 1e−80 94 6261 23648 701118383H1 SOYMON037 g169326 BLASTN 475 1e−30 88 6262 24404 700737869H1 SOYMON012 g169326 BLASTN 460 1e−44 86 6263 3053 701212666H1 SOYMON035 g20468 BLASTN 868 1e−63 84 6264 3053 701212028H1 SOYMON035 g20468 BLASTN 631 1e−61 80 6265 3053 700977561H1 SOYMON009 g20468 BLASTN 841 1e−61 79 6266 3053 700905407H1 SOYMON022 g20468 BLASTN 843 1e−61 84 6267 3053 700792066H1 SOYMON011 g20468 BLASTN 776 1e−55 79 6268 3053 701128564H1 SOYMON037 g20468 BLASTN 708 1e−50 78 6269 3053 700946436H1 SOYMON024 g20468 BLASTN 683 1e−48 75 6270 3053 701137311H1 SOYMON038 g20468 BLASTN 379 1e−39 80 6271 3053 700977732H1 SOYMON009 g20468 BLASTN 279 1e−37 77 6272 32402 700843745H1 SOYMON021 g2150027 BLASTX 164 1e−15 88 6273 7467 700998015H1 SOYMON018 g2150026 BLASTN 600 1e−46 73 6274 7467 701051278H1 SOYMON032 g2150026 BLASTN 594 1e−40 79 6275 7467 700742622H1 SOYMON012 g2150026 BLASTN 582 1e−39 79 6276 7467 700672459H1 SOYMON006 g2911148 BLASTX 201 1e−20 90 6277 7467 700668110H1 SOYMON006 g2911148 BLASTX 201 1e−20 90 6278 7467 701067027H1 SOYMON034 g169326 BLASTN 356 1e−20 78 6279 7467 700740551H1 SOYMON012 g2150027 BLASTX 138 1e−11 60 6280 7507 700725450H1 SOYMON009 g20468 BLASTN 888 1e−65 81 6281 7507 700863501H1 SOYMON027 g20468 BLASTN 873 1e−63 79 6282 7507 700961324H1 SOYMON022 g20468 BLASTN 748 1e−53 77 6283 7507 700648881H1 SOYMON003 g20468 BLASTN 443 1e−46 76 6284 7507 700727322H1 SOYMON009 g2150027 BLASTX 196 1e−19 90 6285 32402 LIB3055-009- LIB3055 g2150028 BLASTN 458 1e−27 80 Q1-N1-E5 6286 7467 LIB3051-044- LIB3051 g169326 BLASTN 633 1e−42 76 Q1-K1-A10 6287 7507 LIB3050-004- LIB3050 g20468 BLASTN 635 1e−42 80 Q1-E1-B1 MAIZE NAD-DEPENDENT MALIC ENZYME 6022 18769 700076676H1 SATMON007 g20469 BLASTX 181 1e−18 77 6023 18769 700155440H1 SATMON007 g20469 BLASTX 140 1e−12 73 6288 -701172938 701172938H2 SATMONN05 g438131 BLASTX 95 1e−18 77 6289 18115 700217870H1 SATMON016 g438131 BLASTX 157 1e−14 84 6290 -700455719 700455719H1 SATMON029 g1129068 BLASTX 137 1e−14 72 SOYBEAN NAD-DEPENDENT MALIC ENZYME 6291 -700565009 700565009H1 SOYMON002 g438131 BLASTX 126 1e−10 73 6292 -701041607 701041607H1 SOYMON029 g437104 BLASTX 124 1e−21 76 6293 -GM32323 LIB3051-012- LIB3051 g438131 BLASTX 152 1e−31 89 Q1-E1-H7 MAIZE PEP CARBOXYKINASE 6294 -700442004 700442004H1 SATMON026 g607751 BLASTN 348 1e−21 71 6295 -700579766 700579766H1 SATMON031 g607751 BLASTN 223 1e−16 79 6296 -700619673 700619673H1 SATMON034 g607751 BLASTN 281 1e−15 87 6297 15221 700620909H1 SATMON034 g607751 BLASTN 657 1e−66 88 6298 15221 700620957H1 SATMON034 g607751 BLASTN 657 1e−51 88 6299 1650 700098127H1 SATMON009 g607751 BLASTN 1241 1e−100 91 6300 1650 700243074H1 SATMON010 g607751 BLASTN 1190 1e−90 92 6301 1650 700098909H1 SATMON009 g607751 BLASTN 662 1e−89 89 6302 1650 700578805H1 SATMON031 g607751 BLASTN 783 1e−84 92 6303 1650 700577590H1 SATMON031 g607751 BLASTN 1116 1e−84 91 6304 1650 700576768H1 SATMON031 g607751 BLASTN 885 1e−83 93 6305 1650 700025522H1 SATMON004 g607751 BLASTN 1097 1e−82 93 6306 1650 700197175H1 SATMON014 g607751 BLASTN 1067 1e−80 93 6307 1650 700432603H1 SATMONN01 g607751 BLASTN 659 1e−76 92 6308 1650 700193379H1 SATMON014 g607751 BLASTN 976 1e−72 91 6309 1650 700196761H1 SATMON014 g607751 BLASTN 718 1e−50 92 6310 1650 700441535H1 SATMON026 g607751 BLASTN 391 1e−36 84 6311 1650 700158221H1 SATMON012 g607751 BLASTN 307 1e−28 92 6312 20890 700101572H1 SATMON009 g607751 BLASTN 1300 1e−99 90 6313 20890 700099023H1 SATMON009 g607751 BLASTN 1139 1e−86 89 6314 20890 700577054H1 SATMON031 g607751 BLASTN 587 1e−79 90 6315 20890 700458441H1 SATMON029 g607751 BLASTN 1025 1e−76 85 6316 22085 700101950H1 SATMON009 g607751 BLASTN 273 1e−19 85 6317 22085 700101726H1 SATMON009 g607751 BLASTN 282 1e−12 92 6318 22085 700045944H1 SATMON004 g607751 BLASTN 268 1e−11 91 6319 22085 700099310H1 SATMON009 g607751 BLASTN 269 1e−11 89 6320 22085 700097484H1 SATMON009 g607751 BLASTN 245 1e−9 88 6321 22085 700101996H1 SATMON009 g607751 BLASTN 245 1e−9 85 6322 28836 700168982H1 SATMON013 g607751 BLASTN 195 1e−9 78 6323 3602 700098761H1 SATMON009 g607751 BLASTN 688 1e−94 87 6324 3602 700240336H1 SATMON010 g607751 BLASTN 1023 1e−76 89 6325 3602 701158475H1 SATMONN04 g607751 BLASTN 907 1e−66 86 6326 8009 700028978H1 SATMON003 g607751 BLASTN 681 1e−83 89 6327 8009 700440427H1 SATMON026 g607751 BLASTN 726 1e−72 89 6328 8009 700440419H1 SATMON026 g607751 BLASTN 715 1e−67 87 6329 8009 700578684H1 SATMON031 g607751 BLASTN 720 1e−66 84 6330 -L1433016 LIB143-017- LIB143 g607751 BLASTN 344 1e−17 77 Q1-E1-G12 6331 -L1892500 LIB189-018- LIB189 g607751 BLASTN 483 1e−29 77 Q1-E1-A7 6332 -L30604864 LIB3060-022- LIB3060 g607751 BLASTN 266 1e−11 89 Q1-K1-A10 6333 1650 LIB3069-045- LIB3069 g607751 BLASTN 1868 1e−146 91 Q1-K1-A5 6334 1650 LIB189-002- LIB189 g607751 BLASTN 1532 1e−118 92 Q1-E1-F5 6335 1650 LIB84-013- LIB84 g607751 BLASTN 1316 1e−100 88 Q1-E1-D8 6336 1650 LIB143-049- LIB143 g607751 BLASTN 1233 1e−93 91 Q1-E1-D10 6337 20890 10-LIB189- LIB189 g607751 BLASTN 1467 1e−113 86 016-Q1-E1-C9 6338 22085 LIB3060-018- LIB3060 g607751 BLASTN 288 1e−41 73 Q1-K1-C8 6339 22085 LIB3060-028- LIB3060 g567102 BLASTX 132 1e−38 66 Q1-K1-F4 6340 22085 LIB143-052- LIB143 g607751 BLASTN 288 1e−32 84 Q1-E1-B12 6341 22085 LIB3060-025- LIB3060 g607751 BLASTN 280 1e−28 85 Q1-K1-F9 6342 22085 LIB3060-005- LIB3060 g607751 BLASTN 280 1e−27 84 Q1-K1-G11 6343 22085 LIB3060-045- LIB3060 g607751 BLASTN 280 1e−22 79 Q1-K1-A8 6344 22085 LIB3060-036- LIB3060 g607751 BLASTN 280 1e−17 85 Q1-K1-G2 6345 22085 LIB3060-045- LIB3060 g607751 BLASTN 280 1e−17 88 Q1-K1-E8 6346 22085 LIB3060-001- LIB3060 g607751 BLASTN 280 1e−12 90 Q1-K2-G11 6347 22085 LIB3060-007- LIB3060 g607751 BLASTN 280 1e−12 92 Q1-K1-A4 6348 22085 LIB3060-007- LIB3060 g607751 BLASTN 273 1e−11 91 Q1-K1-D2 6349 22085 LIB189-007- LIB189 g607751 BLASTN 259 1e−10 88 Q1-E1-H6 6350 28836 LIB143-067- LIB143 g607751 BLASTN 281 1e−12 91 Q1-E1-E12 6351 3602 LIB3060-024- LIB3060 g607751 BLASTN 1188 1e−112 81 Q1-K1-F3 6352 8009 LIB189-023- LIB189 g607751 BLASTN 758 1e−110 85 Q1-E1-H8 6353 8009 LIB3060-013- LIB3060 g607751 BLASTN 1184 1e−99 87 Q1-K1-F1 SOYBEAN PEP CARBOXYKINASE 6354 -700654736 700654736H1 SOYMON004 g567102 BLASTX 204 1e−21 86 6355 -700848574 700848574H1 SOYMON021 g567101 BLASTN 741 1e−52 80 6356 -700866163 700866163H1 SOYMON016 g567102 BLASTX 60 1e−10 71 6357 -700868677 700868677H1 SOYMON016 g914915 BLASTX 163 1e−15 65 6358 -700943040 700943040H1 SOYMON024 g567101 BLASTN 405 1e−23 82 6359 -700972225 700972225H1 SOYMON005 g567101 BLASTN 588 1e−47 82 6360 -700996224 700996224H1 SOYMON018 g567101 BLASTN 563 1e−38 83 6361 -701045039 701045039H1 SOYMON032 g914914 BLASTN 581 1e−54 82 6362 12737 700605402H2 SOYMON004 g567101 BLASTN 809 1e−58 76 6363 12737 700888213H1 SOYMON024 g607751 BLASTN 361 1e−19 75 6364 13320 701040204H1 SOYMON029 g914914 BLASTN 1002 1e−74 81 6365 13320 701042078H1 SOYMON029 g914914 BLASTN 865 1e−63 81 6366 13320 700849715H1 SOYMON021 g914914 BLASTN 745 1e−53 83 6367 17750 700959272H1 SOYMON022 g567102 BLASTX 154 1e−13 53 6368 17750 700961793H1 SOYMON022 g567102 BLASTX 119 1e−9 50 6369 20486 700726640H1 SOYMON009 g567102 BLASTX 131 1e−16 75 6370 24418 700605382H2 SOYMON004 g914914 BLASTN 814 1e−59 76 6371 24418 701052653H1 SOYMON032 g567101 BLASTN 760 1e−54 79 6372 24418 700847843H1 SOYMON021 g567101 BLASTN 447 1e−50 82 6373 24418 701051337H1 SOYMON032 g914914 BLASTN 715 1e−50 78 6374 24418 700656509H1 SOYMON004 g914914 BLASTN 655 1e−45 72 6375 24418 701101473H1 SOYMON028 g567101 BLASTN 417 1e−43 80 6376 24418 701053551H1 SOYMON032 g607752 BLASTX 126 1e−14 72 6377 26845 701046671H1 SOYMON032 g567101 BLASTN 528 1e−35 67 6378 26845 701103555H1 SOYMON028 g607751 BLASTN 352 1e−18 63 6379 -GM20322 LIB3056-013- LIB3056 g567101 BLASTN 766 1e−53 81 Q1-N1-F3 6380 -GM36301 LIB3051-054- LIB3051 g607751 BLASTN 273 1e−11 91 Q1-K1-G11 6381 -GM37519 LIB3051-063- LIB3051 g567101 BLASTN 911 1e−67 81 Q1-K1-D7 6382 11698 LIB3051-065- LIB3051 g567102 BLASTX 167 1e−32 58 Q1-K1-G9 6383 12737 LIB3051-003- LIB3051 g567101 BLASTN 820 1e−58 75 Q1-E1-C4 6384 24418 LIB3051-104- LIB3051 g914914 BLASTN 1096 1e−89 77 Q1-K1-G11 6385 24418 LIB3051-042- LIB3051 g567101 BLASTN 1019 1e−84 78 Q1-K1-C1 6386 24418 LIB3051-116- LIB3051 g914914 BLASTN 918 1e−67 73 Q1-K1-B4 6387 24418 LIB3051-046- LIB3051 g914914 BLASTN 863 1e−65 76 Q1-K1-E11 SOYBEAN PUTATIVE PEP CARBOXYKINASE 6388 -700868431 700868431H1 SOYMON016 g2827717 BLASTX 94 1e−9 81 MAIZE PYRUVATE, PHOSPHATE DIKINASE 6389 -700044189 700044189H1 SATMON004 g168579 BLASTN 155 1e−10 89 6390 -700098830 700098830H1 SATMON009 g257804 BLASTN 317 1e−76 93 6391 -700267212 700267212H1 SATMON017 g168579 BLASTN 1115 1e−84 86 6392 -700268101 700268101H1 SATMON017 g257809 BLASTN 698 1e−66 96 6393 -700404827 700404827H1 SATMON026 g168583 BLASTN 445 1e−57 89 6394 -700426407 700426407H1 SATMONN01 g168579 BLASTN 365 1e−21 81 6395 -700430716 700430716H1 SATMONN01 g22451 BLASTN 210 1e−8 83 6396 -700438208 700438208H1 SATMON026 g168584 BLASTN 325 1e−50 94 6397 -700438250 700438250H1 SATMON026 g168579 BLASTN 263 1e−28 94 6398 -700442440 700442440H1 SATMON026 g168579 BLASTN 492 1e−63 84 6399 -700442486 700442486H1 SATMON026 g168579 BLASTN 399 1e−34 76 6400 -700442534 700442534H1 SATMON026 g168579 BLASTN 280 1e−26 86 6401 -700445755 700445755H1 SATMON027 g168579 BLASTN 537 1e−45 91 6402 -700448312 700448312H1 SATMON027 g168579 BLASTN 201 1e−16 93 6403 -700458259 700458259H1 SATMON029 g168579 BLASTN 635 1e−57 87 6404 -700460850 700460850H1 SATMON031 g168579 BLASTN 227 1e−14 92 6405 -700576979 700576979H1 SATMON031 g168579 BLASTN 239 1e−9 89 6406 -700582461 700582461H1 SATMON031 g168584 BLASTN 310 1e−34 86 6407 -700613790 700613790H1 SATMON033 g168579 BLASTN 473 1e−69 90 6408 -700615033 700615033H1 SATMON033 g168579 BLASTN 1209 1e−94 89 6409 -700807115 700807115H1 SATMON036 g168579 BLASTN 961 1e−71 85 6410 -700807148 700807148H1 SATMON036 g168579 BLASTN 1046 1e−78 85 6411 -700807285 700807285H1 SATMON036 g168579 BLASTN 850 1e−61 81 6412 241 700616008H1 SATMON033 g168579 BLASTN 1750 1e−136 99 6413 241 700084360H1 SATMON011 g168579 BLASTN 1706 1e−133 99 6414 241 700097569H1 SATMON009 g168579 BLASTN 1635 1e−127 100 6415 241 700099686H1 SATMON009 g168579 BLASTN 1540 1e−124 100 6416 241 700097065H1 SATMON009 g168579 BLASTN 1565 1e−124 100 6417 241 700097577H1 SATMON009 g168579 BLASTN 1601 1e−124 99 6418 241 700098157H1 SATMON009 g168579 BLASTN 1588 1e−123 99 6419 241 700095354H1 SATMON008 g168579 BLASTN 1578 1e−122 99 6420 241 700097024H1 SATMON009 g168579 BLASTN 1561 1e−121 98 6421 241 700101705H1 SATMON009 g168579 BLASTN 1563 1e−121 99 6422 241 700100753H1 SATMON009 g168579 BLASTN 1569 1e−121 98 6423 241 700209526H1 SATMON016 g168579 BLASTN 1548 1e−120 98 6424 241 700101967H1 SATMON009 g168579 BLASTN 1550 1e−120 100 6425 241 700100971H1 SATMON009 g168579 BLASTN 1552 1e−120 97 6426 241 700097028H1 SATMON009 g168579 BLASTN 876 1e−119 99 6427 241 700100216H1 SATMON009 g168579 BLASTN 1068 1e−118 98 6428 241 700100408H1 SATMON009 g168579 BLASTN 1413 1e−118 99 6429 241 700098443H1 SATMON009 g168579 BLASTN 1518 1e−117 99 6430 241 700099779H1 SATMON009 g168579 BLASTN 1502 1e−116 97 6431 241 700099086H1 SATMON009 g168579 BLASTN 1503 1e−116 99 6432 241 700101887H1 SATMON009 g168579 BLASTN 1506 1e−116 99 6433 241 700097164H1 SATMON009 g168579 BLASTN 1489 1e−115 98 6434 241 700100751H1 SATMON009 g168579 BLASTN 1492 1e−115 97 6435 241 700101890H1 SATMON009 g168579 BLASTN 1498 1e−115 99 6436 241 700100212H1 SATMON009 g168579 BLASTN 1042 1e−114 99 6437 241 700100040H1 SATMON009 g168579 BLASTN 1484 1e−114 99 6438 241 700101179H1 SATMON009 g168579 BLASTN 1486 1e−114 99 6439 241 700097777H1 SATMON009 g168579 BLASTN 1097 1e−113 97 6440 241 700621494H1 SATMON034 g168579 BLASTN 1184 1e−113 97 6441 241 700621492H1 SATMON034 g168579 BLASTN 1184 1e−113 97 6442 241 700620055H1 SATMON034 g168579 BLASTN 1205 1e−113 98 6443 241 700099278H1 SATMON009 g168579 BLASTN 1468 1e−113 99 6444 241 700100235H1 SATMON009 g168579 BLASTN 1036 1e−112 97 6445 241 700097726H1 SATMON009 g168579 BLASTN 1452 1e−112 99 6446 241 700099458H1 SATMON009 g168579 BLASTN 1452 1e−112 97 6447 241 700101405H1 SATMON009 g168579 BLASTN 1457 1e−112 99 6448 241 700098006H1 SATMON009 g168579 BLASTN 1458 1e−112 98 6449 241 700098988H1 SATMON009 g168579 BLASTN 1460 1e−112 98 6450 241 700101193H1 SATMON009 g168579 BLASTN 1460 1e−112 100 6451 241 700099029H1 SATMON009 g168579 BLASTN 1450 1e−111 100 6452 241 700099494H1 SATMON009 g168579 BLASTN 1451 1e−111 99 6453 241 700624034H1 SATMON034 g168579 BLASTN 887 1e−110 92 6454 241 700099587H1 SATMON009 g168579 BLASTN 1432 1e−110 97 6455 241 700097537H1 SATMON009 g168579 BLASTN 1434 1e−110 98 6456 241 700099280H1 SATMON009 g168579 BLASTN 1437 1e−110 98 6457 241 700099242H1 SATMON009 g168579 BLASTN 924 1e−109 98 6458 241 700097259H1 SATMON009 g168579 BLASTN 1275 1e−109 98 6459 241 700099789H1 SATMON009 g168579 BLASTN 1422 1e−109 96 6460 241 700097672H1 SATMON009 g168579 BLASTN 1425 1e−109 95 6461 241 700099985H1 SATMON009 g168579 BLASTN 870 1e−108 99 6462 241 700045762H1 SATMON004 g168579 BLASTN 1410 1e−108 100 6463 241 700101542H1 SATMON009 g168579 BLASTN 1008 1e−107 98 6464 241 700099788H1 SATMON009 g168579 BLASTN 1255 1e−107 99 6465 241 700265183H1 SATMON017 g168579 BLASTN 1394 1e−107 97 6466 241 700072495H1 SATMON007 g168579 BLASTN 1395 1e−107 96 6467 241 700578123H1 SATMON031 g168579 BLASTN 1398 1e−107 98 6468 241 700445628H1 SATMON027 g168579 BLASTN 1401 1e−107 96 6469 241 700098025H1 SATMON009 g168579 BLASTN 1403 1e−107 98 6470 241 700457276H1 SATMON029 g168579 BLASTN 1380 1e−106 100 6471 241 700045419H1 SATMON004 g168579 BLASTN 1385 1e−106 100 6472 241 700457282H1 SATMON029 g168579 BLASTN 1385 1e−106 100 6473 241 700042861H1 SATMON004 g168579 BLASTN 1387 1e−106 99 6474 241 700099765H1 SATMON009 g168579 BLASTN 1177 1e−105 96 6475 241 700213650H1 SATMON016 g168579 BLASTN 1367 1e−105 99 6476 241 700157249H1 SATMON012 g168579 BLASTN 1370 1e−105 100 6477 241 700441931H1 SATMON026 g168579 BLASTN 1370 1e−105 98 6478 241 700097944H1 SATMON009 g168579 BLASTN 1372 1e−105 97 6479 241 700423208H1 SATMONN01 g168579 BLASTN 630 1e−104 97 6480 241 700442667H1 SATMON026 g168579 BLASTN 1259 1e−104 98 6481 241 700044521H1 SATMON004 g168579 BLASTN 1355 1e−104 100 6482 241 700208177H1 SATMON016 g168579 BLASTN 1365 1e−104 97 6483 241 700444555H1 SATMON027 g168579 BLASTN 1227 1e−103 99 6484 241 700580211H1 SATMON031 g168579 BLASTN 1238 1e−103 99 6485 241 700577814H1 SATMON031 g168579 BLASTN 1345 1e−103 98 6486 241 700100895H1 SATMON009 g168579 BLASTN 1347 1e−103 97 6487 241 700100893H1 SATMON009 g168579 BLASTN 1347 1e−103 98 6488 241 700442655H1 SATMON026 g168579 BLASTN 1351 1e−103 99 6489 241 700101289H1 SATMON009 g168579 BLASTN 1353 1e−103 99 6490 241 700446244H1 SATMON027 g168579 BLASTN 778 1e−102 99 6491 241 700210293H1 SATMON016 g168579 BLASTN 943 1e−102 98 6492 241 700404894H1 SATMON026 g168579 BLASTN 1202 1e−102 97 6493 241 700577581H1 SATMON031 g168579 BLASTN 1331 1e−102 98 6494 241 700041646H1 SATMON004 g168579 BLASTN 1335 1e−102 98 6495 241 700442593H1 SATMON026 g168579 BLASTN 1338 1e−102 99 6496 241 700581301H1 SATMON031 g168579 BLASTN 1338 1e−102 98 6497 241 700043360H1 SATMON004 g168579 BLASTN 1340 1e−102 100 6498 241 700044853H1 SATMON004 g168579 BLASTN 1340 1e−102 100 6499 241 700581894H1 SATMON031 g168579 BLASTN 1342 1e−102 98 6500 241 700582749H1 SATMON031 g168579 BLASTN 853 1e−101 99 6501 241 700046068H1 SATMON004 g168579 BLASTN 864 1e−101 98 6502 241 700045115H1 SATMON004 g168579 BLASTN 1320 1e−101 100 6503 241 700053428H1 SATMON009 g168579 BLASTN 1321 1e−101 99 6504 241 700100830H1 SATMON009 g168579 BLASTN 1321 1e−101 99 6505 241 700441945H1 SATMON026 g168579 BLASTN 1326 1e−101 98 6506 241 700576780H1 SATMON031 g168579 BLASTN 1326 1e−101 97 6507 241 700442663H1 SATMON026 g168579 BLASTN 1326 1e−101 99 6508 241 700439640H1 SATMON026 g168579 BLASTN 1005 1e−100 97 6509 241 700098515H1 SATMON009 g168579 BLASTN 1211 1e−100 97 6510 241 700430478H1 SATMONN01 g168579 BLASTN 1307 1e−100 98 6511 241 700802781H1 SATMON036 g168579 BLASTN 1307 1e−100 99 6512 241 700045313H1 SATMON004 g168579 BLASTN 1316 1e−100 99 6513 241 700045790H1 SATMON004 g168579 BLASTN 1316 1e−100 99 6514 241 700440018H1 SATMON026 g168579 BLASTN 1317 1e−100 99 6515 241 700100827H1 SATMON009 g168579 BLASTN 1317 1e−100 99 6516 241 700617476H1 SATMON033 g168579 BLASTN 558 1e−99 96 6517 241 700577914H1 SATMON031 g168579 BLASTN 1002 1e−99 96 6518 241 700440805H1 SATMON026 g168579 BLASTN 1295 1e−99 100 6519 241 700097121H1 SATMON009 g168579 BLASTN 1295 1e−99 90 6520 241 700043644H1 SATMON004 g168579 BLASTN 1296 1e−99 97 6521 241 700045549H1 SATMON004 g168579 BLASTN 1301 1e−99 99 6522 241 700578928H1 SATMON031 g168579 BLASTN 1303 1e−99 99 6523 241 700467315H1 SATMON025 g168579 BLASTN 490 1e−98 98 6524 241 700583117H1 SATMON031 g168579 BLASTN 955 1e−98 95 6525 241 700801426H1 SATMON036 g168579 BLASTN 1256 1e−98 99 6526 241 700041748H1 SATMON004 g168579 BLASTN 1286 1e−98 97 6527 241 700043365H1 SATMON004 g168579 BLASTN 1294 1e−98 98 6528 241 700042742H1 SATMON004 g168579 BLASTN 1294 1e−98 97 6529 241 700041509H1 SATMON004 g168579 BLASTN 870 1e−97 99 6530 241 700098536H1 SATMON009 g168584 BLASTN 910 1e−97 97 6531 241 700100481H1 SATMON009 g168579 BLASTN 1109 1e−97 93 6532 241 700578290H1 SATMON031 g168579 BLASTN 1232 1e−97 99 6533 241 700045316H1 SATMON004 g168579 BLASTN 1272 1e−97 97 6534 241 700043494H1 SATMON004 g168579 BLASTN 1275 1e−97 97 6535 241 700044584H1 SATMON004 g168579 BLASTN 1276 1e−97 99 6536 241 700619616H1 SATMON034 g168579 BLASTN 1278 1e−97 87 6537 241 700041517H1 SATMON004 g168579 BLASTN 1281 1e−97 96 6538 241 700100133H1 SATMON009 g168579 BLASTN 496 1e−96 94 6539 241 700456453H1 SATMON029 g168579 BLASTN 669 1e−96 97 6540 241 700440516H1 SATMON026 g168579 BLASTN 1015 1e−96 100 6541 241 700042888H1 SATMON004 g168579 BLASTN 1172 1e−96 99 6542 241 700157245H1 SATMON012 g168579 BLASTN 1259 1e−96 98 6543 241 700261321H1 SATMON017 g168579 BLASTN 1261 1e−96 99 6544 241 700045657H1 SATMON004 g168579 BLASTN 1265 1e−96 95 6545 241 700042469H1 SATMON004 g168579 BLASTN 1265 1e−96 98 6546 241 700434549H1 SATMONN01 g168579 BLASTN 1269 1e−96 91 6547 241 700433527H1 SATMONN01 g168579 BLASTN 795 1e−95 99 6548 241 701177258H1 SATMONN05 g168579 BLASTN 900 1e−95 96 6549 241 700440442H1 SATMON026 g168579 BLASTN 997 1e−95 97 6550 241 700432310H1 SATMONN01 g168579 BLASTN 1074 1e−95 97 6551 241 700026635H1 SATMON003 g168579 BLASTN 1077 1e−95 96 6552 241 700043320H1 SATMON004 g168579 BLASTN 1129 1e−95 98 6553 241 700025682H1 SATMON004 g168579 BLASTN 1256 1e−95 98 6554 241 700441415H1 SATMON026 g168579 BLASTN 580 1e−94 96 6555 241 700460762H1 SATMON031 g168579 BLASTN 624 1e−94 97 6556 241 700053387H1 SATMON009 g168584 BLASTN 649 1e−94 96 6557 241 700044829H1 SATMON004 g168579 BLASTN 960 1e−94 100 6558 241 700576848H1 SATMON031 g168579 BLASTN 1207 1e−94 98 6559 241 700195073H1 SATMON014 g168579 BLASTN 1245 1e−94 98 6560 241 700044956H1 SATMON004 g168579 BLASTN 1246 1e−94 97 6561 241 700441974H1 SATMON026 g168579 BLASTN 588 1e−93 97 6562 241 700045323H1 SATMON004 g168579 BLASTN 673 1e−93 98 6563 241 700584010H1 SATMON031 g168579 BLASTN 753 1e−93 92 6564 241 700098611H1 SATMON009 g168579 BLASTN 1137 1e−93 97 6565 241 700043635H1 SATMON004 g168584 BLASTN 1231 1e−93 99 6566 241 700441843H1 SATMON026 g168579 BLASTN 1232 1e−93 98 6567 241 700621537H1 SATMON034 g168579 BLASTN 638 1e−92 93 6568 241 700438416H1 SATMON026 g168579 BLASTN 1013 1e−92 97 6569 241 700043045H1 SATMON004 g168579 BLASTN 1117 1e−92 99 6570 241 700433859H1 SATMONN01 g168579 BLASTN 1148 1e−92 96 6571 241 700580039H1 SATMON031 g168579 BLASTN 1159 1e−92 96 6572 241 700208040H1 SATMON016 g168579 BLASTN 1171 1e−92 98 6573 241 700043891H1 SATMON004 g168579 BLASTN 1211 1e−92 97 6574 241 701175175H1 SATMONN05 g168579 BLASTN 1212 1e−92 98 6575 241 700210840H1 SATMON016 g168579 BLASTN 1214 1e−92 96 6576 241 700086935H1 SATMON011 g168579 BLASTN 1221 1e−92 87 6577 241 700044111H1 SATMON004 g168579 BLASTN 700 1e−91 98 6578 241 700576815H1 SATMON031 g168579 BLASTN 912 1e−91 96 6579 241 700438522H1 SATMON026 g168579 BLASTN 1105 1e−91 97 6580 241 700578239H1 SATMON031 g168579 BLASTN 1119 1e−91 98 6581 241 700044219H1 SATMON004 g168579 BLASTN 1200 1e−91 100 6582 241 700220031H1 SATMON011 g168579 BLASTN 1203 1e−91 96 6583 241 700454149H1 SATMON029 g168579 BLASTN 1203 1e−91 95 6584 241 700578265H1 SATMON031 g168579 BLASTN 1074 1e−90 98 6585 241 700442849H1 SATMON026 g168579 BLASTN 891 1e−89 94 6586 241 700044381H1 SATMON004 g168579 BLASTN 1033 1e−89 95 6587 241 700578031H1 SATMON031 g168579 BLASTN 1175 1e−89 96 6588 241 700802158H1 SATMON036 g168579 BLASTN 1183 1e−89 91 6589 241 700581537H1 SATMON031 g168579 BLASTN 434 1e−88 97 6590 241 700447772H1 SATMON027 g168579 BLASTN 628 1e−88 96 6591 241 700044908H1 SATMON004 g168579 BLASTN 1166 1e−88 97 6592 241 700806626H1 SATMON036 g168579 BLASTN 1167 1e−88 95 6593 241 700580766H1 SATMON031 g168579 BLASTN 1168 1e−88 98 6594 241 700100482H1 SATMON009 g168579 BLASTN 1169 1e−88 87 6595 241 700428285H1 SATMONN01 g168579 BLASTN 707 1e−87 97 6596 241 700158124H1 SATMON012 g168579 BLASTN 918 1e−87 98 6597 241 700439158H1 SATMON026 g168579 BLASTN 922 1e−87 93 6598 241 700577046H1 SATMON031 g168579 BLASTN 989 1e−87 97 6599 241 700098026H1 SATMON009 g168579 BLASTN 1151 1e−87 87 6600 241 700099229H1 SATMON009 g168579 BLASTN 1154 1e−87 98 6601 241 700045027H1 SATMON004 g168579 BLASTN 1162 1e−87 97 6602 241 701177010H1 SATMONN05 g22452 BLASTN 413 1e−86 94 6603 241 700044687H1 SATMON004 g168579 BLASTN 660 1e−86 99 6604 241 700438501H1 SATMON026 g168579 BLASTN 714 1e−86 95 6605 241 700044229H1 SATMON004 g168579 BLASTN 965 1e−86 100 6606 241 700447355H1 SATMON027 g168579 BLASTN 1074 1e−86 96 6607 241 700806248H1 SATMON036 g168579 BLASTN 1082 1e−86 96 6608 241 700044220H1 SATMON004 g168579 BLASTN 1132 1e−85 97 6609 241 700193031H1 SATMON014 g168579 BLASTN 1121 1e−84 92 6610 241 700581571H1 SATMON031 g168584 BLASTN 461 1e−83 95 6611 241 700100987H1 SATMON009 g168579 BLASTN 1006 1e−83 93 6612 241 700439748H1 SATMON026 g168579 BLASTN 1107 1e−83 97 6613 241 700441474H1 SATMON026 g168579 BLASTN 570 1e−82 96 6614 241 700042302H1 SATMON004 g168579 BLASTN 586 1e−82 98 6615 241 700616327H1 SATMON033 g168579 BLASTN 604 1e−82 88 6616 241 700194736H1 SATMON014 g168584 BLASTN 625 1e−82 96 6617 241 700578367H1 SATMON031 g168579 BLASTN 674 1e−82 96 6618 241 700042652H1 SATMON004 g168579 BLASTN 693 1e−82 98 6619 241 700397564H1 SATMONN01 g168579 BLASTN 965 1e−82 89 6620 241 700434288H1 SATMONN01 g168584 BLASTN 1096 1e−82 92 6621 241 700429519H1 SATMONN01 g168579 BLASTN 1098 1e−82 89 6622 241 700438174H1 SATMON026 g168579 BLASTN 1102 1e−82 90 6623 241 700583672H1 SATMON031 g168579 BLASTN 894 1e−81 88 6624 241 700441307H1 SATMON026 g168579 BLASTN 1088 1e−81 99 6625 241 701176710H1 SATMONN05 g22452 BLASTN 477 1e−79 94 6626 241 700581577H1 SATMON031 g168579 BLASTN 551 1e−79 94 6627 241 700428336H1 SATMONN01 g168579 BLASTN 948 1e−79 92 6628 241 700018165H1 SATMON001 g168579 BLASTN 1020 1e−79 98 6629 241 700405414H1 SATMON029 g168579 BLASTN 1058 1e−79 98 6630 241 700239413H1 SATMON010 g168579 BLASTN 965 1e−78 95 6631 241 700581594H1 SATMON031 g168579 BLASTN 607 1e−76 89 6632 241 700433062H1 SATMONN01 g168579 BLASTN 642 1e−76 85 6633 241 700581979H1 SATMON031 g168579 BLASTN 1019 1e−76 85 6634 241 700441332H1 SATMON026 g168579 BLASTN 1023 1e−76 94 6635 241 700441363H1 SATMON026 g168579 BLASTN 1016 1e−75 94 6636 241 700807116H1 SATMON036 g168581 BLASTN 686 1e−74 99 6637 241 700800557H1 SATMON036 g168579 BLASTN 985 1e−73 86 6638 241 700803903H1 SATMON036 g168579 BLASTN 391 1e−72 87 6639 241 700257764H1 SATMON017 g168579 BLASTN 974 1e−72 94 6640 241 700207392H1 SATMON016 g168579 BLASTN 960 1e−71 100 6641 241 700193933H1 SATMON014 g168579 BLASTN 969 1e−71 88 6642 241 700806409H1 SATMON036 g168581 BLASTN 543 1e−69 96 6643 241 700195405H1 SATMON014 g168579 BLASTN 740 1e−69 87 6644 241 700579292H1 SATMON031 g168579 BLASTN 746 1e−69 94 6645 241 700427458H1 SATMONN01 g168584 BLASTN 337 1e−68 88 6646 241 700624196H1 SATMON034 g168579 BLASTN 648 1e−66 90 6647 241 700805096H1 SATMON036 g168579 BLASTN 900 1e−66 86 6648 241 700042161H1 SATMON004 g168579 BLASTN 903 1e−66 91 6649 241 700578768H1 SATMON031 g168584 BLASTN 908 1e−66 93 6650 241 700802865H1 SATMON036 g168584 BLASTN 705 1e−65 94 6651 241 700580152H1 SATMON031 g168579 BLASTN 863 1e−63 96 6652 241 700041938H1 SATMON004 g168584 BLASTN 845 1e−61 100 6653 241 700196549H1 SATMON014 g168579 BLASTN 848 1e−61 91 6654 241 700425162H1 SATMONN01 g22451 BLASTN 805 1e−60 100 6655 241 701160579H1 SATMONN04 g168579 BLASTN 380 1e−59 96 6656 241 700456514H1 SATMON029 g168579 BLASTN 822 1e−59 92 6657 241 700441507H1 SATMON026 g168579 BLASTN 697 1e−58 96 6658 241 700099603H1 SATMON009 g168579 BLASTN 804 1e−58 98 6659 241 700442758H1 SATMON026 g168579 BLASTN 326 1e−56 90 6660 241 700804296H1 SATMON036 g168579 BLASTN 687 1e−54 84 6661 241 700438664H1 SATMON026 g168579 BLASTN 277 1e−53 96 6662 241 700441510H1 SATMON026 g168579 BLASTN 388 1e−52 96 6663 241 700428514H1 SATMONN01 g168579 BLASTN 491 1e−52 96 6664 241 700101932H1 SATMON009 g168579 BLASTN 384 1e−50 92 6665 241 700262656H1 SATMON017 g168579 BLASTN 542 1e−49 93 6666 241 700583279H1 SATMON031 g168579 BLASTN 449 1e−47 95 6667 241 700624652H1 SATMON034 g168579 BLASTN 623 1e−47 96 6668 241 700612451H1 SATMON033 g168579 BLASTN 672 1e−47 89 6669 241 700335324H1 SATMON019 g168581 BLASTN 637 1e−46 71 6670 241 700440390H1 SATMON026 g168579 BLASTN 361 1e−45 95 6671 241 700097825H1 SATMON009 g168579 BLASTN 650 1e−45 100 6672 241 701163821H1 SATMONN04 g168581 BLASTN 606 1e−44 98 6673 241 700438560H1 SATMON026 g168584 BLASTN 623 1e−43 96 6674 241 700805587H1 SATMON036 g168579 BLASTN 632 1e−43 84 6675 241 700100859H1 SATMON009 g168579 BLASTN 612 1e−42 97 6676 241 700580595H1 SATMON031 g168579 BLASTN 295 1e−39 81 6677 241 700441529H1 SATMON026 g168584 BLASTN 302 1e−37 97 6678 241 700045548H1 SATMON004 g22451 BLASTN 511 1e−36 99 6679 241 700097365H1 SATMON009 g168579 BLASTN 544 1e−36 97 6680 241 700424468H1 SATMONN01 g168579 BLASTN 547 1e−36 94 6681 241 700457633H1 SATMON029 g168584 BLASTN 275 1e−35 96 6682 241 700425102H1 SATMONN01 g168579 BLASTN 472 1e−33 92 6683 241 700097811H1 SATMON009 g168579 BLASTN 501 1e−32 87 6684 241 700404795H1 SATMON026 g168584 BLASTN 483 1e−31 98 6685 241 700431218H1 SATMONN01 g168579 BLASTN 302 1e−29 96 6686 241 700097835H1 SATMON009 g168579 BLASTN 337 1e−29 89 6687 241 700100627H1 SATMON009 g168579 BLASTN 444 1e−28 94 6688 241 700618263H1 SATMON033 g168579 BLASTN 286 1e−27 88 6689 241 700583801H1 SATMON031 g168579 BLASTN 350 1e−26 95 6690 241 700099807H1 SATMON009 g168579 BLASTN 233 1e−24 94 6691 241 700097573H1 SATMON009 g168579 BLASTN 305 1e−23 92 6692 241 700427553H1 SATMONN01 g168584 BLASTN 344 1e−23 93 6693 241 700098562H1 SATMON009 g168579 BLASTN 309 1e−16 95 6694 241 700799964H1 SATMON036 g168584 BLASTN 234 1e−13 94 6695 3862 700266534H1 SATMON017 g257804 BLASTN 923 1e−77 97 6696 3862 700455813H1 SATMON029 g257804 BLASTN 879 1e−66 98 6697 3862 700099255H1 SATMON009 g168579 BLASTN 460 1e−29 91 6698 5767 700098424H1 SATMON009 g22449 BLASTN 1555 1e−120 98 6699 5767 700099971H1 SATMON009 g168583 BLASTN 1468 1e−113 96 6700 5767 700044869H1 SATMON004 g168583 BLASTN 1242 1e−99 98 6701 5767 700097037H1 SATMON009 g168579 BLASTN 1264 1e−96 89 6702 5767 700095363H1 SATMON008 g168583 BLASTN 310 1e−78 97 6703 5767 700101364H1 SATMON009 g22449 BLASTN 1006 1e−75 94 6704 5767 700101568H1 SATMON009 g22449 BLASTN 1013 1e−75 95 6705 5767 700045180H1 SATMON004 g22449 BLASTN 901 1e−74 90 6706 5767 700042559H1 SATMON004 g22449 BLASTN 998 1e−74 94 6707 5767 700045393H1 SATMON004 g22449 BLASTN 865 1e−63 100 6708 5767 700099658H1 SATMON009 g22449 BLASTN 531 1e−35 92 6709 -L1433809 LIB143-024- LIB143 g168579 BLASTN 256 1e−23 81 Q1-E1-F11 6710 -L30592709 LIB3059-017- LIB3059 g2443401 BLASTN 431 1e−27 68 Q1-K1-F2 6711 -L30593789 LIB3059-022- LIB3059 g168584 BLASTN 361 1e−21 89 Q1-K1-D6 6712 -L30594314 LIB3059-032- LIB3059 g168579 BLASTN 488 1e−29 63 Q1-K1-G4 6713 -L30594987 LIB3059-056- LIB3059 g168579 BLASTN 406 1e−41 73 Q1-K1-G11 6714 -L30596613 LIB3059-054- LIB3059 g168579 BLASTN 568 1e−52 78 Q1-K1-F4 6715 -L30602598 LIB3060-018- LIB3060 g168579 BLASTN 580 1e−79 73 Q1-K1-B4 6716 -L30602793 LIB3060-014- LIB3060 g168583 BLASTN 513 1e−62 77 Q1-K1-C6 6717 -L30602820 LIB3060-017- LIB3060 g168579 BLASTN 151 1e−12 89 Q1-K1-B1 6718 -L30603538 LIB3060-045- LIB3060 g168583 BLASTN 382 1e−34 88 Q1-K1-E12 6719 -L30603998 LIB3060-036- LIB3060 g168579 BLASTN 678 1e−90 82 Q1-K1-H4 6720 -L30605229 LIB3060-050- LIB3060 g168579 BLASTN 305 1e−16 80 Q1-K1-D5 6721 -L30611520 LIB3061-002- LIB3061 g168581 BLASTN 492 1e−41 82 Q1-K2-D12 6722 -L30615750 LIB3061-042- LIB3061 g168579 BLASTN 223 1e−11 96 Q1-K1-H11 6723 -L30783291 LIB3078-051- LIB3078 g168579 BLASTN 538 1e−70 73 Q1-K1-G3 6724 -L30784553 LIB3078-011- LIB3078 g168579 BLASTN 671 1e−90 83 Q1-K1-B7 6725 -L361816 LIB36-020- LIB36 g168579 BLASTN 738 1e−69 82 Q1-E1-A10 6726 -L362168 LIB36-005- LIB36 g168579 BLASTN 304 1e−15 72 Q1-E1-D11 6727 -L362639 LIB36-007- LIB36 g168584 BLASTN 332 1e−36 86 Q1-E1-F2 6728 -L831870 LIB83-009- LIB83 g168579 BLASTN 250 1e−11 100 Q1-E1-E9 6729 -L831984 LIB83-010- LIB83 g168584 BLASTN 382 1e−41 89 Q1-E1-B1 6730 241 LIB36-016- LIB36 g168579 BLASTN 2261 1e−179 99 Q2-E2-E10 6731 241 LIB3060-003- LIB3060 g168579 BLASTN 2186 1e−173 99 Q1-K1-C3 6732 241 LIB3078-052- LIB3078 g168579 BLASTN 2188 1e−173 99 Q1-K1-H5 6733 241 LIB3078-033- LIB3078 g168579 BLASTN 2176 1e−172 98 Q1-K1-A12 6734 241 LIB36-016- LIB36 g168579 BLASTN 2164 1e−171 98 Q2-E2-C3 6735 241 LIB3060-054- LIB3060 g168579 BLASTN 1973 1e−168 97 Q1-K1-E4 6736 241 LIB36-016- LIB36 g168579 BLASTN 2130 1e−168 98 Q2-E2-C5 6737 241 LIB36-014- LIB36 g168579 BLASTN 1968 1e−167 96 Q1-E1-D2 6738 241 LIB3059-058- LIB3059 g168579 BLASTN 2112 1e−167 98 Q1-K1-A12 6739 241 LIB3060-006- LIB3060 g168579 BLASTN 1699 1e−165 97 Q1-K1-C1 6740 241 LIB3060-016- LIB3060 g168579 BLASTN 2051 1e−165 99 Q1-K1-F8 6741 241 LIB3060-045- LIB3060 g168579 BLASTN 2098 1e−165 97 Q1-K1-E3 6742 241 LIB3060-026- LIB3060 g168579 BLASTN 1162 1e−164 94 Q1-K1-D6 6743 241 LIB3060-012- LIB3060 g168579 BLASTN 1897 1e−164 98 Q1-K1-A7 6744 241 LIB83-003- LIB83 g168579 BLASTN 2077 1e−164 96 Q1-E1-G2 6745 241 LIB143-022- LIB143 g168579 BLASTN 2087 1e−164 98 Q1-E1-G5 6746 241 LIB3060-044- LIB3060 g168579 BLASTN 1768 1e−163 95 Q1-K1-F6 6747 241 LIB3060-025- LIB3060 g168579 BLASTN 2058 1e−162 96 Q1-K1-B10 6748 241 LIB36-005- LIB36 g168579 BLASTN 2059 1e−162 97 Q1-E1-C7 6749 241 LIB3060-052- LIB3060 g168579 BLASTN 1831 1e−161 97 Q1-K1-D5 6750 241 LIB3059-024- LIB3059 g168579 BLASTN 1932 1e−161 99 Q1-K1-F6 6751 241 LIB36-002- LIB36 g168579 BLASTN 2051 1e−161 98 Q1-E1-B10 6752 241 LIB3060-052- LIB3060 g168579 BLASTN 1740 1e−160 97 Q1-K1-E8 6753 241 LIB3060-016- LIB3060 g168579 BLASTN 2030 1e−160 97 Q1-K1-G8 6754 241 LIB84-004- LIB84 g168579 BLASTN 2034 1e−160 97 Q1-E1-C3 6755 241 LIB3060-051- LIB3060 g168579 BLASTN 2037 1e−160 98 Q1-K1-E9 6756 241 LIB84-013- LIB84 g168579 BLASTN 2018 1e−159 98 Q1-E1-A5 6757 241 LIB3078-002- LIB3078 g168579 BLASTN 2027 1e−159 97 Q1-K1-E2 6758 241 LIB189-006- LIB189 g168579 BLASTN 1791 1e−158 99 Q1-E1-G6 6759 241 LIB3060-044- LIB3060 g168579 BLASTN 1692 1e−157 98 Q1-K1-F8 6760 241 LIB36-004- LIB36 g168579 BLASTN 1892 1e−157 98 Q1-E1-B11 6761 241 LIB3078-013- LIB3078 g168579 BLASTN 1853 1e−156 97 Q1-K1-H10 6762 241 LIB36-015- LIB36 g168579 BLASTN 1988 1e−156 98 Q1-E1-F9 6763 241 LIB189-020- LIB189 g168579 BLASTN 1972 1e−155 98 Q1-E1-G9 6764 241 LIB36-004- LIB36 g168579 BLASTN 1972 1e−155 99 Q1-E1-F10 6765 241 LIB3060-005- LIB3060 g168579 BLASTN 1974 1e−155 99 Q1-K1-B6 6766 241 LIB3060-052- LIB3060 g168579 BLASTN 1979 1e−155 94 Q1-K1-H7 6767 241 LIB189-007- LIB189 g168579 BLASTN 1130 1e−154 99 Q1-E1-G11 6768 241 LIB83-006- LIB83 g168579 BLASTN 1964 1e−154 98 Q1-E1-C7 6769 241 LIB189-009- LIB189 g168579 BLASTN 1405 1e−150 97 Q1-E1-G9 6770 241 LIB3060-036- LIB3060 g168579 BLASTN 1910 1e−150 94 Q1-K1-H3 6771 241 LIB189-013- LIB189 g168579 BLASTN 1732 1e−149 93 Q1-E1-D10 6772 241 LIB36-014- LIB36 g168579 BLASTN 1519 1e−147 95 Q1-E1-D12 6773 241 LIB3078-055- LIB3078 g168579 BLASTN 1860 1e−146 90 Q1-K1-E2 6774 241 LIB3060-004- LIB3060 g168579 BLASTN 1830 1e−143 97 Q1-K1-D9 6775 241 LIB189-020- LIB189 g168579 BLASTN 1823 1e−142 92 Q1-E1-G4 6776 241 LIB3060-008- LIB3060 g168579 BLASTN 1511 1e−140 90 Q1-K1-D10 6777 241 LIB189-008- LIB189 g168579 BLASTN 1379 1e−139 95 Q1-E1-B5 6778 241 LIB3059-040- LIB3059 g168579 BLASTN 1437 1e−139 91 Q1-K1-E1 6779 241 LIB3078-051- LIB3078 g168579 BLASTN 1474 1e−139 96 Q1-K1-G2 6780 241 LIB84-029- LIB84 g168579 BLASTN 1508 1e−136 98 Q1-E1-E6 6781 241 LIB36-004- LIB36 g168579 BLASTN 1310 1e−134 94 Q1-E1-D1 6782 241 LIB3059-012- LIB3059 g168579 BLASTN 1720 1e−134 89 Q1-K1-D10 6783 241 LIB3059-044- LIB3059 g168579 BLASTN 1725 1e−134 87 Q1-K1-E2 6784 241 LIB3059-043- LIB3059 g168579 BLASTN 1588 1e−133 87 Q1-K1-F7 6785 241 LIB189-008- LIB189 g168579 BLASTN 1705 1e−133 91 Q1-E1-H1 6786 241 LIB83-003- LIB83 g168579 BLASTN 1422 1e−131 97 Q1-E1-D3 6787 241 LIB189-002- LIB189 g168579 BLASTN 1656 1e−131 97 Q1-E1-C11 6788 241 LIB36-002- LIB36 g168579 BLASTN 1546 1e−129 96 Q1-E1-F3 6789 241 LIB189-015- LIB189 g168579 BLASTN 1062 1e−127 94 Q1-E1-F3 6790 241 LIB189-013- LIB189 g168579 BLASTN 1639 1e−127 97 Q1-E1-F6 6791 241 LIB3061-007- LIB3061 g168579 BLASTN 1625 1e−126 85 Q1-K1-A1 6792 241 LIB3060-054- LIB3060 g168579 BLASTN 879 1e−123 89 Q1-K1-D4 6793 241 LIB3078-028- LIB3078 g168579 BLASTN 1066 1e−123 93 Q1-K1-A6 6794 241 LIB3059-047- LIB3059 g168579 BLASTN 1576 1e−122 85 Q1-K1-H7 6795 241 LIB36-021- LIB36 g168579 BLASTN 1465 1e−121 100 Q1-E1-F1 6796 241 LIB3059-002- LIB3059 g168579 BLASTN 1273 1e−119 81 Q1-K2-A4 6797 241 LIB189-015- LIB189 g168579 BLASTN 1530 1e−118 94 Q1-E1-G8 6798 241 LIB189-007- LIB189 g168579 BLASTN 1517 1e−117 96 Q1-E1-F9 6799 241 LIB3079-013- LIB3079 g168579 BLASTN 1367 1e−115 90 Q1-K1-G8 6800 241 LIB36-015- LIB36 g168579 BLASTN 1333 1e−113 95 Q1-E1-D2 6801 241 LIB3059-018- LIB3059 g168579 BLASTN 1210 1e−112 86 Q1-K1-H2 6802 241 LIB3078-007- LIB3078 g168579 BLASTN 508 1e−111 90 Q1-K1-E1 6803 241 LIB3060-038- LIB3060 g168579 BLASTN 1443 1e−111 98 Q1-K1-H3 6804 241 LIB36-020- LIB36 g168579 BLASTN 1446 1e−111 95 Q1-E1-A9 6805 241 LIB3061-026- LIB3061 g168579 BLASTN 1435 1e−110 86 Q1-K1-D7 6806 241 LIB36-021- LIB36 g168579 BLASTN 1381 1e−109 96 Q1-E1-G7 6807 241 LIB3059-028- LIB3059 g168579 BLASTN 884 1e−108 88 Q1-K1-G7 6808 241 LIB189-029- LIB189 g168579 BLASTN 982 1e−108 87 Q1-E1-D4 6809 241 LIB3060-020- LIB3060 g168579 BLASTN 1053 1e−108 77 Q1-K1-F2 6810 241 LIB36-007- LIB36 g168579 BLASTN 1348 1e−108 94 Q1-E1-E9 6811 241 LIB3059-017- LIB3059 g168579 BLASTN 1096 1e−106 87 Q1-K1-C3 6812 241 LIB3061-051- LIB3061 g168581 BLASTN 931 1e−104 90 Q1-K1-H5 6813 241 LIB3061-009- LIB3061 g168579 BLASTN 1032 1e−102 76 Q1-K1-F12 6814 241 LIB3061-041- LIB3061 g168579 BLASTN 1326 1e−101 88 Q1-K1-C5 6815 241 LIB36-013- LIB36 g168579 BLASTN 1328 1e−101 91 Q1-E1-B6 6816 241 LIB84-016- LIB84 g168579 BLASTN 1308 1e−100 97 Q1-E1-A7 6817 241 LIB84-002- LIB84 g168579 BLASTN 716 1e−99 90 Q1-E1-D6 6818 241 LIB3060-039- LIB3060 g168579 BLASTN 1166 1e−99 92 Q1-K1-E5 6819 241 LIB3078-011- LIB3078 g168579 BLASTN 558 1e−95 84 Q1-K1-E7 6820 241 LIB3060-052- LIB3060 g168579 BLASTN 596 1e−95 89 Q1-K1-H8 6821 241 LIB3060-026- LIB3060 g168579 BLASTN 817 1e−94 82 Q1-K1-D7 6822 241 LIB3059-003- LIB3059 g168579 BLASTN 954 1e−93 86 Q1-K1-F1 6823 241 LIB189-006- LIB189 g22451 BLASTN 1136 1e−88 97 Q1-E1-C4 6824 241 LIB189-029- LIB189 g168579 BLASTN 746 1e−87 92 Q1-E1-C2 6825 241 LIB84-003- LIB84 g168584 BLASTN 1143 1e−86 99 Q1-E1-C2 6826 241 LIB36-014- LIB36 g168579 BLASTN 760 1e−83 97 Q1-E1-A2 6827 241 LIB3078-011- LIB3078 g22451 BLASTN 1085 1e−83 100 Q1-K1-D6 6828 241 LIB3059-031- LIB3059 g168581 BLASTN 914 1e−81 93 Q1-K1-E3 6829 241 LIB189-023- LIB189 g168581 BLASTN 755 1e−80 100 Q1-E1-E7 6830 241 LIB83-009- LIB83 g168579 BLASTN 1003 1e−74 92 Q1-E1-D12 6831 241 LIB83-010- LIB83 g168584 BLASTN 546 1e−65 98 Q1-E1-G9 6832 241 LIB189-017- LIB189 g22451 BLASTN 822 1e−61 93 Q1-E1-A5 6833 241 LIB3061-002- LIB3061 g168579 BLASTN 421 1e−57 87 Q1-K1-D12 6834 241 LIB3059-058- LIB3059 g168579 BLASTN 624 1e−55 86 Q1-K1-A4 6835 241 LIB3059-023- LIB3059 g168579 BLASTN 728 1e−51 85 Q1-K1-C3 6836 241 LIB189-027- LIB189 g168579 BLASTN 649 1e−49 87 Q1-E1-F4 6837 241 LIB3059-020- LIB3059 g22389 BLASTN 475 1e−48 91 Q1-K1-E10 6838 241 LIB3060-045- LIB3060 g168579 BLASTN 569 1e−47 89 Q1-K1-H10 6839 241 LIB84-003- LIB84 g22451 BLASTN 668 1e−47 90 Q1-E1-A10 6840 241 LIB3059-037- LIB3059 g22389 BLASTN 475 1e−35 91 Q1-K1-H8 6841 5767 LIB3060-051- LIB3060 g22449 BLASTN 1640 1e−164 99 Q1-K1-C1 6842 5767 LIB3060-015- LIB3060 g168583 BLASTN 1920 1e−162 99 Q1-K1-G11 6843 5767 LIB3060-017- LIB3060 g168583 BLASTN 2060 1e−162 100 Q1-K1-A8 6844 5767 LIB3060-014- LIB3060 g22449 BLASTN 1933 1e−159 97 Q1-K1-C3 6845 5767 LIB3060-010- LIB3060 g22449 BLASTN 1285 1e−156 99 Q1-K1-H5 6846 5767 LIB3060-045- LIB3060 g22449 BLASTN 1020 1e−76 95 Q1-K1-C7 6847 5767 LIB3060-027- LIB3060 g22449 BLASTN 1025 1e−76 95 Q1-K1-E7 SOYBEAN PYRUVATE, PHOSPHATE DIKINASE 6848 -700646607 700646607H1 SOYMON014 g18461 BLASTN 947 1e−70 81 6849 30854 700787466H2 SOYMON011 g577775 BLASTN 825 1e−59 80 6850 30854 LIB3054-008- LIB3054 g577775 BLASTN 1279 1e−97 80 Q1-N1-C5 MAIZE PYROPHOSPHATASE 6851 -700043816 700043816H1 SATMON004 g1049254 BLASTN 476 1e−30 76 6852 -700049210 700049210H1 SATMON003 g1747293 BLASTN 216 1e−10 85 6853 -700098741 700098741H1 SATMON009 g1747293 BLASTN 1093 1e−82 85 6854 -700100718 700100718H1 SATMON009 g1747293 BLASTN 595 1e−40 86 6855 -700105040 700105040H1 SATMON010 g1747293 BLASTN 463 1e−28 76 6856 -700150777 700150777H1 SATMON007 g1747293 BLASTN 708 1e−50 89 6857 -700155610 700155610H1 SATMON007 g1049254 BLASTN 311 1e−15 64 6858 -700163331 700163331H1 SATMON013 g534915 BLASTN 751 1e−53 77 6859 -700171438 700171438H1 SATMON013 g2258073 BLASTN 256 1e−10 76 6860 -700193866 700193866H1 SATMON014 g166633 BLASTN 494 1e−32 64 6861 -700202576 700202576H1 SATMON003 g2668746 BLASTX 214 1e−23 84 6862 -700206487 700206487H1 SATMON003 g2570501 BLASTX 174 1e−17 86 6863 -700216624 700216624H1 SATMON016 g1747293 BLASTN 936 1e−82 84 6864 -700217292 700217292H1 SATMON016 g2668746 BLASTX 214 1e−23 100 6865 -700240889 700240889H1 SATMON010 g2570500 BLASTN 639 1e−47 84 6866 -700242309 700242309H1 SATMON010 g1747293 BLASTN 621 1e−42 69 6867 -700347658 700347658H1 SATMON023 g2668746 BLASTX 215 1e−23 95 6868 -700349391 700349391H1 SATMON023 g1049255 BLASTX 174 1e−17 52 6869 -700427206 700427206H1 SATMONN01 g1049254 BLASTN 292 1e−33 90 6870 -700451045 700451045H1 SATMON028 g1049255 BLASTX 55 1e−10 72 6871 -700454151 700454151H1 SATMON029 g2668745 BLASTN 172 1e−10 90 6872 -700454532 700454532H1 SATMON029 g2668745 BLASTN 259 1e−38 93 6873 -700475488 700475488H1 SATMON025 g1747293 BLASTN 1126 1e−84 90 6874 -700552133 700552133H1 SATMON022 g457744 BLASTX 176 1e−19 68 6875 -700571086 700571086H1 SATMON030 g1747293 BLASTN 1429 1e−110 88 6876 -700572341 700572341H1 SATMON030 g1747293 BLASTN 475 1e−70 89 6877 -700611864 700611864H1 SATMON022 g2668745 BLASTN 203 1e−9 84 6878 -701166871 701166871H1 SATMONN04 g1049255 BLASTX 105 1e−13 72 6879 107 700622451H1 SATMON034 g2668745 BLASTN 1645 1e−129 100 6880 107 700571235H1 SATMON030 g2668745 BLASTN 1406 1e−125 98 6881 107 700266126H1 SATMON017 g2668745 BLASTN 1145 1e−121 100 6882 107 700621607H1 SATMON034 g2668745 BLASTN 1375 1e−121 99 6883 107 700345080H1 SATMON021 g2668745 BLASTN 1195 1e−117 100 6884 107 700624257H1 SATMON034 g2668745 BLASTN 825 1e−115 100 6885 107 700030359H1 SATMON003 g2668745 BLASTN 1470 1e−114 100 6886 107 700214462H1 SATMON016 g2668745 BLASTN 1223 1e−110 98 6887 107 700356050H1 SATMON024 g2668745 BLASTN 1430 1e−110 100 6888 107 701181128H1 SATMONN06 g2668745 BLASTN 1368 1e−105 98 6889 107 700349795H1 SATMON023 g2668745 BLASTN 1370 1e−105 95 6890 107 700473278H1 SATMON025 g2668745 BLASTN 1355 1e−104 100 6891 107 700157057H1 SATMON012 g2668745 BLASTN 1345 1e−103 100 6892 107 700622505H1 SATMON034 g2668745 BLASTN 762 1e−100 96 6893 107 700219661H1 SATMON011 g2668745 BLASTN 942 1e−98 99 6894 107 700619032H1 SATMON034 g2668745 BLASTN 989 1e−98 96 6895 107 700620065H1 SATMON034 g2668745 BLASTN 1069 1e−98 94 6896 107 700569179H1 SATMON030 g2668745 BLASTN 1233 1e−97 98 6897 107 700156773H1 SATMON012 g2668745 BLASTN 1276 1e−97 99 6898 107 700207120H1 SATMON017 g2668745 BLASTN 740 1e−96 99 6899 107 700030407H1 SATMON003 g2668745 BLASTN 480 1e−95 98 6900 107 700457309H1 SATMON029 g2668745 BLASTN 979 1e−95 99 6901 107 700195681H1 SATMON014 g2668745 BLASTN 1246 1e−95 99 6902 107 700444838H1 SATMON027 g2668745 BLASTN 1249 1e−95 96 6903 107 700581619H1 SATMON031 g2668745 BLASTN 943 1e−94 96 6904 107 700351021H1 SATMON023 g2668745 BLASTN 853 1e−91 92 6905 107 700205723H1 SATMON003 g2668745 BLASTN 1138 1e−91 95 6906 107 700159712H1 SATMON012 g2668745 BLASTN 1199 1e−91 94 6907 107 700158937H1 SATMON012 g2668745 BLASTN 1132 1e−90 96 6908 107 700336255H1 SATMON019 g2668745 BLASTN 489 1e−85 94 6909 107 700422922H1 SATMONN01 g2668745 BLASTN 642 1e−84 95 6910 107 700347429H1 SATMON023 g2668745 BLASTN 891 1e−83 92 6911 107 700350695H1 SATMON023 g2668745 BLASTN 960 1e−83 91 6912 107 700212988H1 SATMON016 g2668745 BLASTN 988 1e−82 96 6913 107 700345278H1 SATMON021 g2668745 BLASTN 989 1e−82 95 6914 107 700264475H1 SATMON017 g2668745 BLASTN 1089 1e−82 99 6915 107 700211923H1 SATMON016 g2668745 BLASTN 991 1e−81 94 6916 107 700620974H1 SATMON034 g2668745 BLASTN 907 1e−80 92 6917 107 700156401H1 SATMON012 g2668745 BLASTN 1058 1e−79 90 6918 107 700172547H1 SATMON013 g2668745 BLASTN 1042 1e−78 96 6919 107 700552384H1 SATMON022 g2668745 BLASTN 916 1e−76 96 6920 107 700219926H1 SATMON011 g2668745 BLASTN 1005 1e−75 100 6921 107 700357492H1 SATMON024 g2668745 BLASTN 610 1e−74 99 6922 107 700343365H1 SATMON021 g2668745 BLASTN 891 1e−74 94 6923 107 700018618H1 SATMON001 g2668745 BLASTN 1001 1e−74 93 6924 107 700570755H1 SATMON030 g2668745 BLASTN 845 1e−71 93 6925 107 700194777H1 SATMON014 g2668745 BLASTN 940 1e−69 100 6926 107 700453790H1 SATMON029 g2668745 BLASTN 925 1e−68 92 6927 107 700197306H1 SATMON014 g2668745 BLASTN 928 1e−68 85 6928 107 700355750H1 SATMON024 g2668745 BLASTN 393 1e−66 93 6929 107 700172940H1 SATMON013 g2668745 BLASTN 902 1e−66 97 6930 107 700102133H1 SATMON010 g2668745 BLASTN 850 1e−62 100 6931 107 700350332H1 SATMON023 g2668745 BLASTN 539 1e−57 97 6932 107 700450285H1 SATMON028 g2668745 BLASTN 750 1e−53 100 6933 107 700165003H1 SATMON013 g2668745 BLASTN 548 1e−52 83 6934 107 700016136H1 SATMON001 g2668745 BLASTN 527 1e−50 85 6935 107 700171557H1 SATMON013 g2668745 BLASTN 714 1e−50 95 6936 107 700238156H1 SATMON010 g2668745 BLASTN 715 1e−50 96 6937 107 700425175H1 SATMONN01 g2668745 BLASTN 698 1e−49 94 6938 107 700354402H1 SATMON024 g2668745 BLASTN 616 1e−48 91 6939 107 700159204H1 SATMON012 g2668745 BLASTN 617 1e−42 94 6940 107 700623602H1 SATMON034 g2668745 BLASTN 460 1e−38 100 6941 107 700612844H1 SATMON033 g2668745 BLASTN 421 1e−36 84 6942 107 700621062H2 SATMON034 g2668745 BLASTN 285 1e−25 89 6943 107 700335685H1 SATMON019 g2668745 BLASTN 339 1e−25 91 6944 1381 700454845H1 SATMON029 g1747293 BLASTN 746 1e−72 85 6945 1381 700455149H1 SATMON029 g1747293 BLASTN 836 1e−66 84 6946 1381 700455537H1 SATMON029 g1747293 BLASTN 330 1e−29 80 6947 1381 700615620H1 SATMON033 g1747294 BLASTX 105 1e−16 98 6948 1381 700454648H1 SATMON029 g1747293 BLASTN 288 1e−15 78 6949 13843 700334949H1 SATMON019 g2570500 BLASTN 680 1e−55 83 6950 13843 700346817H1 SATMON021 g2570500 BLASTN 705 1e−54 83 6951 13843 700103380H1 SATMON010 g2570500 BLASTN 710 1e−54 83 6952 13843 700348280H1 SATMON023 g2570500 BLASTN 669 1e−51 83 6953 13843 700453203H1 SATMON028 g2570500 BLASTN 659 1e−50 82 6954 13843 700381101H1 SATMON023 g2570500 BLASTN 621 1e−47 82 6955 13843 700347617H1 SATMON023 g2570500 BLASTN 592 1e−44 85 6956 13843 700043259H1 SATMON004 g2570500 BLASTN 530 1e−39 84 6957 13843 701184447H1 SATMONN06 g2570500 BLASTN 481 1e−35 78 6958 18427 700355977H1 SATMON024 g1747295 BLASTN 1056 1e−81 92 6959 18427 700265262H1 SATMON017 g1747295 BLASTN 626 1e−77 90 6960 20656 700075743H1 SATMON007 g1747295 BLASTN 734 1e−52 87 6961 20656 700571658H1 SATMON030 g1747295 BLASTN 480 1e−29 84 6962 21076 700088795H1 SATMON011 g1049254 BLASTN 420 1e−24 64 6963 21076 700241354H1 SATMON010 g166634 BLASTX 201 1e−20 58 6964 21267 700050595H1 SATMON003 g1747293 BLASTN 445 1e−32 83 6965 21267 700090051H1 SATMON011 g1747293 BLASTN 239 1e−23 74 6966 24066 700423113H1 SATMONN01 g457744 BLASTX 124 1e−23 54 6967 24266 700577157H1 SATMON031 g2570500 BLASTN 1001 1e−74 89 6968 2531 700099364H1 SATMON009 g2570500 BLASTN 669 1e−51 86 6969 2531 700336387H1 SATMON019 g2570500 BLASTN 389 1e−47 85 6970 2531 700217095H1 SATMON016 g2570500 BLASTN 451 1e−33 86 6971 2531 700155869H1 SATMON007 g2570500 BLASTN 385 1e−27 89 6972 2531 700575534H1 SATMON030 g2570500 BLASTN 365 1e−26 88 6973 2531 700163562H1 SATMON013 g2570501 BLASTX 145 1e−24 94 6974 2544 700076138H1 SATMON007 g1747295 BLASTN 1334 1e−102 90 6975 2544 700381158H1 SATMON023 g1747295 BLASTN 962 1e−92 89 6976 2544 700050877H1 SATMON003 g1747295 BLASTN 933 1e−85 87 6977 2544 700450220H1 SATMON028 g1747295 BLASTN 1105 1e−85 90 6978 2544 700050516H1 SATMON003 g1747295 BLASTN 574 1e−75 91 6979 2544 700620486H1 SATMON034 g1049254 BLASTN 734 1e−54 94 6980 293 700474550H1 SATMON025 g1049254 BLASTN 1359 1e−110 97 6981 293 700218212H1 SATMON016 g1049254 BLASTN 1411 1e−108 99 6982 293 700468143H1 SATMON025 g1049254 BLASTN 1397 1e−107 97 6983 293 700101735H1 SATMON009 g1049254 BLASTN 1364 1e−104 98 6984 293 700454255H1 SATMON029 g1049254 BLASTN 1333 1e−102 97 6985 293 700051815H1 SATMON003 g1049254 BLASTN 1256 1e−95 96 6986 293 700623739H1 SATMON034 g1049254 BLASTN 1245 1e−94 92 6987 293 700577880H1 SATMON031 g1049254 BLASTN 1218 1e−92 94 6988 293 700457170H1 SATMON029 g1049254 BLASTN 1198 1e−91 93 6989 293 700476606H1 SATMON025 g1049254 BLASTN 1204 1e−91 92 6990 293 700620920H1 SATMON034 g1049254 BLASTN 1179 1e−89 94 6991 293 700100479H1 SATMON009 g1747293 BLASTN 1164 1e−88 87 6992 293 700551082H1 SATMON022 g1747293 BLASTN 1151 1e−87 92 6993 293 700156615H1 SATMON012 g1049254 BLASTN 1152 1e−87 94 6994 293 700161538H1 SATMON012 g1049254 BLASTN 1143 1e−86 98 6995 293 700157125H1 SATMON012 g1049254 BLASTN 1115 1e−84 93 6996 293 700173068H1 SATMON013 g1049254 BLASTN 1121 1e−84 94 6997 293 700050620H1 SATMON003 g1049254 BLASTN 481 1e−82 90 6998 293 700622261H1 SATMON034 g1049254 BLASTN 614 1e−76 97 6999 293 700043120H1 SATMON004 g1747293 BLASTN 1014 1e−75 87 7000 293 700215855H1 SATMON016 g1049254 BLASTN 985 1e−73 100 7001 293 700098048H1 SATMON009 g1049254 BLASTN 912 1e−72 95 7002 293 700021133H1 SATMON001 g1049254 BLASTN 546 1e−71 93 7003 293 700021236H1 SATMON001 g1049254 BLASTN 963 1e−71 90 7004 293 700431153H1 SATMONN01 g1747293 BLASTN 510 1e−68 85 7005 293 700441425H1 SATMON026 g1747293 BLASTN 569 1e−67 82 7006 293 700160941H1 SATMON012 g1747293 BLASTN 504 1e−66 87 7007 293 700160760H1 SATMON012 g1747293 BLASTN 906 1e−66 86 7008 293 700439081H1 SATMON026 g1049254 BLASTN 909 1e−66 92 7009 293 700444194H1 SATMON027 g1747293 BLASTN 887 1e−65 84 7010 293 700217965H1 SATMON016 g1747293 BLASTN 855 1e−62 91 7011 293 700456962H1 SATMON029 g1747293 BLASTN 496 1e−61 78 7012 293 700438388H1 SATMON026 g1049254 BLASTN 668 1e−52 98 7013 293 700623436H1 SATMON034 g1747293 BLASTN 696 1e−49 82 7014 293 700472039H1 SATMON025 g1049254 BLASTN 629 1e−43 98 7015 293 700624180H1 SATMON034 g1747293 BLASTN 395 1e−35 82 7016 293 700162157H1 SATMON012 g1747294 BLASTX 185 1e−18 97 7017 293 700162372H1 SATMON012 g1049255 BLASTX 132 1e−10 100 7018 3131 700624482H1 SATMON034 g1747295 BLASTN 1155 1e−95 87 7019 3131 700075221H1 SATMON007 g1747295 BLASTN 1228 1e−93 89 7020 3131 700213731H1 SATMON016 g1747295 BLASTN 1095 1e−84 89 7021 3131 700215864H1 SATMON016 g1747295 BLASTN 1120 1e−84 90 7022 3131 700465076H1 SATMON025 g1747295 BLASTN 1084 1e−81 89 7023 3131 700077092H1 SATMON007 g1747295 BLASTN 998 1e−74 83 7024 32364 700204306H1 SATMON003 g2668745 BLASTN 471 1e−28 74 7025 32671 700451634H1 SATMON028 g1747293 BLASTN 578 1e−73 87 7026 32856 700166756H1 SATMON013 g534915 BLASTN 744 1e−53 76 7027 32856 700042535H1 SATMON004 g534915 BLASTN 644 1e−44 73 7028 337 700242009H1 SATMON010 g1747293 BLASTN 1049 1e−78 90 7029 337 700624035H1 SATMON034 g1747293 BLASTN 1008 1e−75 85 7030 337 700266136H1 SATMON017 g1747293 BLASTN 999 1e−74 84 7031 337 700220713H1 SATMON011 g1747293 BLASTN 752 1e−56 90 7032 3384 700237775H1 SATMON010 g2258073 BLASTN 911 1e−67 81 7033 3384 700342456H1 SATMON021 g2258073 BLASTN 648 1e−64 78 7034 3384 700073654H1 SATMON007 g2668745 BLASTN 860 1e−63 78 7035 3384 700577805H1 SATMON031 g2258073 BLASTN 840 1e−61 78 7036 3384 700028881H1 SATMON003 g534915 BLASTN 835 1e−60 78 7037 3384 700215076H1 SATMON016 g534915 BLASTN 824 1e−59 78 7038 3384 700017479H1 SATMON001 g534915 BLASTN 766 1e−55 80 7039 3384 700204495H1 SATMON003 g534915 BLASTN 373 1e−51 81 7040 3384 700196795H1 SATMON014 g2570500 BLASTN 579 1e−39 80 7041 3384 700018612H1 SATMON001 g2668745 BLASTN 518 1e−34 76 7042 3384 700102142H1 SATMON010 g2668745 BLASTN 539 1e−34 78 7043 3384 700348430H1 SATMON023 g534915 BLASTN 489 1e−30 78 7044 3384 700439515H1 SATMON026 g534915 BLASTN 437 1e−27 75 7045 3384 700074977H1 SATMON007 g534915 BLASTN 434 1e−25 76 7046 3384 700023120H1 SATMON003 g534916 BLASTX 208 1e−22 78 7047 3384 700615213H1 SATMON033 g2570501 BLASTX 125 1e−21 93 7048 3384 700074109H1 SATMON007 g2668746 BLASTX 197 1e−20 72 7049 3384 700026094H1 SATMON003 g534916 BLASTX 184 1e−18 75 7050 3384 700549517H1 SATMON022 g2668746 BLASTX 172 1e−17 75 7051 3384 700030347H1 SATMON003 g2668746 BLASTX 171 1e−16 77 7052 3384 700221176H1 SATMON011 g2668746 BLASTX 171 1e−16 77 7053 3384 700433360H1 SATMONN01 g2668746 BLASTX 95 1e−13 74 7054 3817 700047790H1 SATMON003 g1747295 BLASTN 412 1e−57 85 7055 3817 700266224H1 SATMON017 g1747295 BLASTN 473 1e−50 85 7056 3817 700209335H1 SATMON016 g1747295 BLASTN 503 1e−42 86 7057 3817 700089769H1 SATMON011 g1747295 BLASTN 487 1e−40 85 7058 3817 700151762H1 SATMON007 g1747295 BLASTN 457 1e−37 87 7059 3817 700449259H1 SATMON028 g1747295 BLASTN 339 1e−19 81 7060 5000 700026151H1 SATMON003 g2903 BLASTX 261 1e−28 54 7061 5000 700347165H1 SATMON021 g2624379 BLASTX 223 1e−24 51 7062 5000 700430341H1 SATMONN01 g2903 BLASTX 185 1e−18 56 7063 5000 700457781H1 SATMON029 g2903 BLASTX 133 1e−16 49 7064 5861 700104993H1 SATMON010 g2258073 BLASTN 456 1e−27 73 7065 5861 700203452H1 SATMON003 g2258073 BLASTN 428 1e−26 72 7066 5861 700105585H1 SATMON010 g534916 BLASTX 149 1e−13 84 7067 5861 700240805H1 SATMON010 g534916 BLASTX 131 1e−11 82 7068 5861 700030336H1 SATMON003 g534916 BLASTX 120 1e−9 82 7069 5861 700217859H1 SATMON016 g534916 BLASTX 120 1e−9 82 7070 6315 700473069H1 SATMON025 g1747295 BLASTN 1200 1e−91 89 7071 6315 700151232H1 SATMON007 g1747295 BLASTN 1130 1e−85 90 7072 6315 700103088H1 SATMON010 g1747295 BLASTN 1132 1e−85 88 7073 6315 700450086H2 SATMON028 g1747295 BLASTN 591 1e−84 90 7074 6315 700458843H1 SATMON029 g1747295 BLASTN 822 1e−67 89 7075 6315 700165715H1 SATMON013 g1747295 BLASTN 494 1e−63 89 7076 6315 700352887H1 SATMON024 g1747295 BLASTN 606 1e−41 86 7077 707 700206525H1 SATMON003 g1747295 BLASTN 1386 1e−106 91 7078 707 700096774H1 SATMON008 g1747295 BLASTN 1264 1e−96 90 7079 707 700466734H1 SATMON025 g1747295 BLASTN 1078 1e−89 90 7080 707 700332548H1 SATMON019 g1747295 BLASTN 1179 1e−89 89 7081 707 700085122H1 SATMON011 g1747295 BLASTN 1171 1e−88 92 7082 707 700207180H1 SATMON017 g1747295 BLASTN 1159 1e−87 88 7083 707 700333910H1 SATMON019 g1747295 BLASTN 1134 1e−85 92 7084 707 700223824H1 SATMON011 g1747295 BLASTN 1122 1e−84 91 7085 707 700222034H1 SATMON011 g1747295 BLASTN 1102 1e−82 88 7086 707 700570554H1 SATMON030 g1747295 BLASTN 848 1e−81 86 7087 707 700241783H1 SATMON010 g1747295 BLASTN 1090 1e−81 89 7088 707 700224305H1 SATMON011 g1747295 BLASTN 1031 1e−77 85 7089 707 700458382H1 SATMON029 g1747295 BLASTN 993 1e−73 89 7090 707 700151266H1 SATMON007 g1747295 BLASTN 671 1e−47 86 7091 707 700470565H1 SATMON025 g1747295 BLASTN 404 1e−46 86 7092 707 700207802H1 SATMON016 g1747295 BLASTN 543 1e−43 87 7093 7540 700049926H1 SATMON003 g1747295 BLASTN 718 1e−50 87 7094 7540 700458612H1 SATMON029 g1747295 BLASTN 670 1e−46 83 7095 -L1431590 LIB143-006- LIB143 g16347 BLASTN 286 1e−13 61 Q1-E1-C9 7096 -L1433414 LIB143-026- LIB143 g2258073 BLASTN 480 1e−29 70 Q1-E1-C3 7097 -L1482832 LIB148-009- LIB148 g2258073 BLASTN 1086 1e−81 78 Q1-E1-D8 7098 -L30593394 LIB3059-029- LIB3059 g1747295 BLASTN 488 1e−91 82 Q1-K1-A12 7099 -L30593582 LIB3059-031- LIB3059 g1747293 BLASTN 807 1e−71 86 Q1-K1-C7 7100 -L30674379 LIB3067-042- LIB3067 g2668745 BLASTN 305 1e−21 68 Q1-K1-H8 7101 -L30675338 LIB3067-035- LIB3067 g1747293 BLASTN 436 1e−25 80 Q1-K1-H12 7102 -L30784040 LIB3078-029- LIB3078 g1747293 BLASTN 523 1e−53 70 Q1-K1-D6 7103 107 LIB3059-036- LIB3059 g2668745 BLASTN 1965 1e−166 100 Q1-K1-B10 7104 107 LIB3061-035- LIB3061 g2668745 BLASTN 948 1e−138 93 Q1-K1-C9 7105 107 LIB3061-032- LIB3061 g2668745 BLASTN 1685 1e−138 96 Q1-K1-A12 7106 107 LIB3062-044- LIB3062 g2668745 BLASTN 1492 1e−134 95 Q1-K1-F8 7107 107 LIB3068-025- LIB3068 g2668745 BLASTN 1687 1e−132 96 Q1-K1-E5 7108 107 LIB3067-022- LIB3067 g2668745 BLASTN 1581 1e−128 91 Q1-K1-D11 7109 107 LIB3067-016- LIB3067 g2668745 BLASTN 1305 1e−126 97 Q1-K1-G4 7110 107 LIB3067-029- LIB3067 g2668745 BLASTN 1560 1e−125 90 Q1-K1-C6 7111 107 LIB189-031- LIB189 g2668745 BLASTN 897 1e−81 85 Q1-E1-D3 7112 24066 LIB3069-047- LIB3069 g166634 BLASTX 173 1e−45 55 Q1-K1-C4 7113 24266 LIB3069-006- LIB3069 g2570500 BLASTN 717 1e−57 83 Q1-K1-F4 7114 293 LIB3060-032- LIB3060 g1049254 BLASTN 2144 1e−170 97 Q1-K1-D3 7115 293 LIB3066-051- LIB3066 g1049254 BLASTN 1603 1e−158 99 Q1-K1-D3 7116 293 LIB3060-026- LIB3060 g1049254 BLASTN 1642 1e−155 92 Q1-K1-G5 7117 293 LIB143-018- LIB143 g1049254 BLASTN 1249 1e−151 99 Q1-E1-D7 7118 293 LIB189-005- LIB189 g1049254 BLASTN 1911 1e−150 98 Q1-E1-G2 7119 293 LIB3059-035- LIB3059 g1049254 BLASTN 1860 1e−146 89 Q1-K1-G7 7120 293 LIB3060-013- LIB3060 g1049254 BLASTN 1236 1e−144 95 Q1-K1-D3 7121 293 LIB3060-010- LIB3060 g1049254 BLASTN 1171 1e−142 90 Q1-K1-G9 7122 293 LIB143-031- LIB143 g1049254 BLASTN 1777 1e−139 97 Q1-E1-F9 7123 293 LIB3067-034- LIB3067 g1049254 BLASTN 1558 1e−121 93 Q1-K1-B4 7124 293 LIB3067-010- LIB3067 g1049254 BLASTN 901 1e−120 90 Q1-K1-A11 7125 293 LIB3060-015- LIB3060 g1049254 BLASTN 1309 1e−106 87 Q1-K1-G3 7126 293 LIB3059-024- LIB3059 g1049254 BLASTN 1255 1e−95 98 Q1-K1-G11 7127 293 LIB3060-038- LIB3060 g1049254 BLASTN 1109 1e−83 87 Q1-K1-B1 7128 293 LIB143-008- LIB143 g1747293 BLASTN 1042 1e−77 85 Q1-E1-B6 7129 293 LIB143-021- LIB143 g1747293 BLASTN 951 1e−70 84 Q1-E1-A12 7130 293 LIB143-037- LIB143 g1747293 BLASTN 858 1e−68 89 Q1-E1-C3 7131 293 LIB3079-004- LIB3079 g1747293 BLASTN 826 1e−59 83 Q1-K1-D5 7132 293 LIB143-028- LIB143 g1747293 BLASTN 598 1e−40 88 Q1-E1-F3 7133 293 LIB3068-043- LIB3068 g633598 BLASTN 552 1e−34 78 Q1-K1-A2 7134 3131 LIB3066-031- LIB3066 g1747295 BLASTN 1114 1e−98 85 Q1-K1-E3 7135 31637 LIB143-001- LIB143 g1747293 BLASTN 472 1e−74 81 Q1-E1-G11 7136 32364 LIB3066-001- LIB3066 g2668745 BLASTN 612 1e−40 73 Q1-K1-B7 7137 32671 LIB143-061- LIB143 g1747293 BLASTN 1414 1e−116 85 Q1-E1-E10 7138 32671 LIB189-020- LIB189 g1747293 BLASTN 1281 1e−97 86 Q1-E1-C10 7139 32856 LIB189-028- LIB189 g534915 BLASTN 986 1e−73 73 Q1-E1-C4 7140 3384 LIB143-026- LIB143 g534915 BLASTN 1284 1e−98 78 Q1-E1-C1 7141 3384 LIB3068-013- LIB3068 g534915 BLASTN 1074 1e−80 78 Q1-K1-H2 7142 3384 LIB3062-033- LIB3062 g2668745 BLASTN 1009 1e−75 76 Q1-K1-D2 7143 3384 LIB3062-057- LIB3062 g2668745 BLASTN 801 1e−58 73 Q1-K1-B7 7144 3384 LIB3062-001- LIB3062 g16347 BLASTN 802 1e−57 77 Q1-K2-H5 7145 3384 LIB189-022- LIB189 g2668745 BLASTN 646 1e−43 75 Q1-E1-D5 7146 3384 LIB189-012- LIB189 g2570501 BLASTX 138 1e−32 72 Q1-E1-F4 7147 5000 LIB36-015- LIB36 g2624379 BLASTX 236 1e−41 51 Q1-E1-D6 7148 5000 LIB83-016- LIB83 g4198 BLASTN 534 1e−33 61 Q1-E1-H7 7149 707 LIB148-019- LIB148 g1747295 BLASTN 1506 1e−116 89 Q1-E1-H8 7150 707 LIB3066-040- LIB3066 g1747295 BLASTN 1459 1e−112 82 Q1-K1-D6 7151 707 LIB148-004- LIB148 g1747295 BLASTN 1268 1e−109 84 Q1-E1-B10 7152 707 LIB3068-036- LIB3068 g1747295 BLASTN 889 1e−102 83 Q1-K1-A10 7153 7540 LIB143-025- LIB143 g1747295 BLASTN 903 1e−66 86 Q1-E1-C10 7154 7540 LIB148-033- LIB148 g1747295 BLASTN 857 1e−65 87 Q1-E1-A7 SOYBEAN PYROPHOSPHATASE 7155 -700651291 700651291H1 SOYMON003 g1049254 BLASTN 732 1e−52 84 7156 -700652792 700652792H1 SOYMON003 g2653445 BLASTN 474 1e−39 88 7157 -700656683 700656683H1 SOYMON004 g1747293 BLASTN 679 1e−59 84 7158 -700660662 700660662H1 SOYMON004 g16347 BLASTN 540 1e−36 79 7159 -700744202 700744202H1 SOYMON013 g485741 BLASTN 554 1e−44 74 7160 -700755514 700755514H1 SOYMON014 g1747293 BLASTN 743 1e−53 78 7161 -700837007 700837007H1 SOYMON020 g16347 BLASTN 776 1e−55 78 7162 -700865679 700865679H1 SOYMON016 g2653445 BLASTN 250 1e−36 92 7163 -700890647 700890647H1 SOYMON024 g790474 BLASTN 826 1e−60 81 7164 -700942978 700942978H1 SOYMON024 g790478 BLASTN 605 1e−63 82 7165 -700944280 700944280H1 SOYMON024 g790479 BLASTX 119 1e−10 76 7166 -700974544 700974544H1 SOYMON005 g1103711 BLASTN 854 1e−62 83 7167 -700984449 700984449H1 SOYMON009 g1103711 BLASTN 287 1e−12 71 7168 -700989248 700989248H1 SOYMON011 g534915 BLASTN 276 1e−14 67 7169 -701002440 701002440H1 SOYMON018 g2653445 BLASTN 784 1e−56 76 7170 -701003295 701003295H1 SOYMON019 g1049255 BLASTX 73 1e−8 53 7171 -701012101 701012101H1 SOYMON019 g2653445 BLASTN 592 1e−40 77 7172 -701097188 701097188H1 SOYMON028 g2653445 BLASTN 557 1e−37 75 7173 -701105007 701105007H1 SOYMON036 g2653445 BLASTN 455 1e−61 86 7174 -701106870 701106870H1 SOYMON036 g790478 BLASTN 623 1e−47 75 7175 -701122796 701122796H1 SOYMON037 g2258074 BLASTX 71 1e−15 73 7176 -701124682 701124682H1 SOYMON037 g485743 BLASTN 713 1e−50 81 7177 -701132123 701132123H1 SOYMON038 g790478 BLASTN 627 1e−43 81 7178 -701136557 701136557H1 SOYMON038 g16347 BLASTN 376 1e−33 77 7179 -701148551 701148551H1 SOYMON031 g2653445 BLASTN 756 1e−54 78 7180 -701206188 701206188H1 SOYMON035 g166633 BLASTN 399 1e−48 81 7181 -701211207 701211207H1 SOYMON035 g2653445 BLASTN 387 1e−28 77 7182 11662 700987644H1 SOYMON009 g1747294 BLASTX 122 1e−17 60 7183 13047 700955418H1 SOYMON022 g2653445 BLASTN 585 1e−82 91 7184 13047 701054053H1 SOYMON032 g2653445 BLASTN 1080 1e−81 87 7185 13047 700846717H1 SOYMON021 g2653445 BLASTN 1000 1e−79 91 7186 13047 700952212H1 SOYMON022 g2653445 BLASTN 1055 1e−79 90 7187 13047 701156608H1 SOYMON031 g2653445 BLASTN 648 1e−78 91 7188 13047 700959847H1 SOYMON022 g2653445 BLASTN 932 1e−76 91 7189 13047 700986383H1 SOYMON009 g2653445 BLASTN 1029 1e−76 87 7190 13047 700892594H1 SOYMON024 g2653445 BLASTN 1005 1e−74 87 7191 13047 700995882H1 SOYMON011 g2653445 BLASTN 515 1e−68 90 7192 13047 701099843H1 SOYMON028 g2653445 BLASTN 850 1e−61 90 7193 14021 700973215H1 SOYMON005 g2668745 BLASTN 435 1e−39 80 7194 14021 701109310H1 SOYMON036 g2668745 BLASTN 281 1e−25 83 7195 14021 700847609H1 SOYMON021 g534916 BLASTX 98 1e−12 74 7196 14580 700952058H1 SOYMON022 g2653445 BLASTN 954 1e−70 88 7197 14580 700756103H1 SOYMON014 g2653445 BLASTN 562 1e−66 84 7198 15316 700847173H1 SOYMON021 g534916 BLASTX 123 1e−10 66 7199 15316 700847165H1 SOYMON021 g534916 BLASTX 121 1e−9 66 7200 15698 700844601H1 SOYMON021 g2653445 BLASTN 976 1e−72 91 7201 15698 700904602H1 SOYMON022 g2653445 BLASTN 466 1e−62 85 7202 15698 701002118H1 SOYMON018 g2653445 BLASTN 860 1e−62 87 7203 16 701044831H1 SOYMON032 g485744 BLASTX 163 1e−17 73 7204 16 700891764H1 SOYMON024 g790479 BLASTX 172 1e−16 68 7205 16 700953633H1 SOYMON022 g485744 BLASTX 161 1e−15 73 7206 16 700753981H1 SOYMON014 g485744 BLASTX 159 1e−14 70 7207 16 701104248H1 SOYMON036 g485744 BLASTX 57 1e−8 68 7208 1820 700888545H1 SOYMON024 g2653445 BLASTN 271 1e−39 84 7209 1820 700954577H1 SOYMON022 g2653445 BLASTN 177 1e−37 80 7210 1820 700869270H1 SOYMON016 g2653445 BLASTN 173 1e−16 80 7211 1820 700792533H1 SOYMON017 g2653445 BLASTN 182 1e−15 80 7212 1820 700734996H1 SOYMON010 g2653445 BLASTN 173 1e−14 78 7213 19232 701061126H1 SOYMON033 g790474 BLASTN 935 1e−69 81 7214 19232 700962864H1 SOYMON022 g790474 BLASTN 874 1e−64 82 7215 20872 700754883H1 SOYMON014 g790478 BLASTN 824 1e−59 81 7216 20872 700971147H1 SOYMON005 g1103711 BLASTN 564 1e−54 79 7217 20885 700904547H1 SOYMON022 g485743 BLASTN 971 1e−72 86 7218 20885 700665391H1 SOYMON005 g485743 BLASTN 969 1e−71 86 7219 20885 700941185H1 SOYMON024 g2653445 BLASTN 868 1e−63 83 7220 20885 700660695H1 SOYMON004 g2653445 BLASTN 825 1e−59 85 7221 20885 701127185H1 SOYMON037 g1747293 BLASTN 463 1e−54 83 7222 24940 701209525H1 SOYMON035 g2653445 BLASTN 789 1e−56 91 7223 24940 701213556H1 SOYMON035 g2653445 BLASTN 574 1e−38 93 7224 27239 700668618H1 SOYMON006 g1049255 BLASTX 179 1e−17 61 7225 2813 700797861H1 SOYMON017 g16347 BLASTN 731 1e−52 79 7226 2813 700944850H1 SOYMON024 g2570500 BLASTN 738 1e−52 82 7227 2813 701056207H1 SOYMON032 g2570500 BLASTN 556 1e−46 80 7228 2813 700605115H2 SOYMON003 g2570500 BLASTN 478 1e−42 80 7229 2813 700897063H1 SOYMON027 g2570500 BLASTN 596 1e−40 80 7230 2813 700561829H1 SOYMON002 g2570500 BLASTN 570 1e−38 80 7231 2813 701204883H1 SOYMON035 g2668745 BLASTN 545 1e−36 77 7232 2813 700754984H1 SOYMON014 g2570500 BLASTN 527 1e−35 75 7233 2813 700854552H1 SOYMON023 g2570500 BLASTN 536 1e−35 79 7234 2813 700873337H1 SOYMON018 g2570500 BLASTN 505 1e−33 75 7235 2813 700873349H1 SOYMON018 g2570500 BLASTN 506 1e−33 75 7236 2813 700952403H1 SOYMON022 g2668745 BLASTN 499 1e−32 76 7237 2813 700846561H1 SOYMON021 g2570500 BLASTN 488 1e−31 75 7238 2813 700953987H1 SOYMON022 g2570500 BLASTN 461 1e−29 75 7239 2813 700568667H1 SOYMON002 g2570500 BLASTN 296 1e−24 79 7240 2813 700895231H1 SOYMON024 g2258074 BLASTX 207 1e−22 80 7241 2813 701101791H1 SOYMON028 g2668746 BLASTX 147 1e−13 77 7242 4106 701011114H1 SOYMON019 g2653445 BLASTN 904 1e−76 90 7243 4106 700674046H1 SOYMON007 g2653445 BLASTN 989 1e−73 90 7244 4106 700967038H1 SOYMON029 g2653445 BLASTN 963 1e−71 90 7245 4106 700740792H1 SOYMON012 g2653445 BLASTN 911 1e−67 90 7246 4106 700872817H1 SOYMON018 g2653445 BLASTN 903 1e−66 89 7247 4106 700738286H1 SOYMON012 g2653446 BLASTX 95 1e−10 91 7248 4845 700566516H1 SOYMON002 g2653445 BLASTN 1358 1e−104 94 7249 4845 700978728H1 SOYMON009 g2653445 BLASTN 917 1e−88 95 7250 4845 700907549H1 SOYMON022 g2653445 BLASTN 1168 1e−88 94 7251 4845 700908149H1 SOYMON022 g2653445 BLASTN 1156 1e−87 92 7252 4845 700559351H1 SOYMON001 g2653445 BLASTN 973 1e−86 90 7253 4845 700898914H1 SOYMON027 g2653445 BLASTN 1140 1e−86 93 7254 4845 700946269H1 SOYMON024 g2653445 BLASTN 1132 1e−85 91 7255 4845 701011513H1 SOYMON019 g2653445 BLASTN 1124 1e−84 92 7256 4845 700785951H2 SOYMON011 g2653445 BLASTN 1114 1e−83 92 7257 4845 701003561H1 SOYMON019 g2653445 BLASTN 1093 1e−82 92 7258 4845 700755340H1 SOYMON014 g2653445 BLASTN 1097 1e−82 93 7259 4845 700756774H1 SOYMON014 g2653445 BLASTN 950 1e−81 92 7260 4845 700564820H1 SOYMON002 g2653445 BLASTN 989 1e−81 87 7261 4845 700902381H1 SOYMON027 g2653445 BLASTN 1055 1e−79 95 7262 4845 700970334H1 SOYMON005 g2653445 BLASTN 978 1e−77 86 7263 4845 700656490H1 SOYMON004 g2653445 BLASTN 941 1e−73 91 7264 4845 700871681H1 SOYMON018 g2653445 BLASTN 974 1e−72 92 7265 4845 701153255H1 SOYMON031 g2653445 BLASTN 758 1e−65 94 7266 4845 701049483H1 SOYMON032 g2653445 BLASTN 865 1e−65 88 7267 4845 700796611H1 SOYMON017 g2653445 BLASTN 577 1e−59 86 7268 4845 700863103H1 SOYMON023 g2653445 BLASTN 771 1e−59 91 7269 4845 700795148H1 SOYMON017 g2653445 BLASTN 631 1e−57 83 7270 4845 701099340H1 SOYMON028 g2653445 BLASTN 678 1e−47 86 7271 4845 701097793H1 SOYMON028 g2653445 BLASTN 571 1e−38 88 7272 5440 701049119H1 SOYMON032 g2653445 BLASTN 1116 1e−84 89 7273 5440 701135152H1 SOYMON038 g2653445 BLASTN 703 1e−72 90 7274 5440 701001376H1 SOYMON018 g2653445 BLASTN 611 1e−67 89 7275 5440 701011545H1 SOYMON019 g2653445 BLASTN 907 1e−66 87 7276 5440 700738622H1 SOYMON012 g2653445 BLASTN 827 1e−60 88 7277 5440 700844506H1 SOYMON021 g2653445 BLASTN 838 1e−60 87 7278 5440 700547904H1 SOYMON001 g2653445 BLASTN 820 1e−59 87 7279 5440 701136362H1 SOYMON038 g2653445 BLASTN 825 1e−59 85 7280 5440 700794050H1 SOYMON017 g2653445 BLASTN 793 1e−57 84 7281 5440 700952580H1 SOYMON022 g2653445 BLASTN 798 1e−57 88 7282 5440 700563827H1 SOYMON002 g2653445 BLASTN 735 1e−56 82 7283 5440 700952567H1 SOYMON022 g2653445 BLASTN 783 1e−56 88 7284 5440 700953831H1 SOYMON022 g2653445 BLASTN 746 1e−53 87 7285 5440 700749982H1 SOYMON013 g2653445 BLASTN 397 1e−50 87 7286 5440 700686154H1 SOYMON008 g2653445 BLASTN 458 1e−48 84 7287 5440 700904783H1 SOYMON022 g2653445 BLASTN 461 1e−48 88 7288 5440 700952870H1 SOYMON022 g2653445 BLASTN 685 1e−48 87 7289 5440 700961948H1 SOYMON022 g2653445 BLASTN 675 1e−47 82 7290 5440 701210118H1 SOYMON035 g2653445 BLASTN 418 1e−45 85 7291 5440 700906779H1 SOYMON022 g2653445 BLASTN 631 1e−43 84 7292 5440 700833390H1 SOYMON019 g2653445 BLASTN 239 1e−36 87 7293 5440 700990989H1 SOYMON011 g2653445 BLASTN 545 1e−36 85 7294 5440 701103017H1 SOYMON028 g2653445 BLASTN 439 1e−27 85 7295 5440 700978736H1 SOYMON009 g2653446 BLASTX 124 1e−16 57 7296 7894 700795920H1 SOYMON017 g2653445 BLASTN 1016 1e−75 87 7297 7894 700888375H1 SOYMON024 g2653445 BLASTN 742 1e−66 88 7298 8040 701121224H1 SOYMON037 g534915 BLASTN 298 1e−14 77 7299 8040 700743066H1 SOYMON012 g2668746 BLASTX 140 1e−12 80 7300 8531 701005139H1 SOYMON019 g2258073 BLASTN 871 1e−63 79 7301 8531 701008308H1 SOYMON019 g534915 BLASTN 789 1e−57 76 7302 8531 700559054H1 SOYMON001 g2570500 BLASTN 790 1e−57 77 7303 8531 700790983H1 SOYMON011 g2258073 BLASTN 431 1e−52 77 7304 8531 701007949H1 SOYMON019 g2570500 BLASTN 404 1e−41 70 7305 8531 701123827H1 SOYMON037 g534915 BLASTN 436 1e−26 75 7306 8531 701013616H1 SOYMON019 g534915 BLASTN 431 1e−25 78 7307 8531 701013624H1 SOYMON019 g534916 BLASTX 210 1e−22 84 7308 8531 700888553H1 SOYMON024 g534916 BLASTX 174 1e−17 91 7309 8531 701106256H1 SOYMON036 g534916 BLASTX 174 1e−17 84 7310 8531 701214976H1 SOYMON035 g534916 BLASTX 165 1e−16 88 7311 8531 700565624H1 SOYMON002 g2570501 BLASTX 169 1e−16 85 7312 8531 701121092H1 SOYMON037 g2570501 BLASTX 110 1e−15 60 7313 8531 700788808H2 SOYMON011 g534916 BLASTX 159 1e−15 88 7314 8531 701099192H1 SOYMON028 g534916 BLASTX 159 1e−15 96 7315 8531 700889521H1 SOYMON024 g534916 BLASTX 162 1e−15 90 7316 8531 700971218H1 SOYMON005 g534916 BLASTX 137 1e−12 90 7317 8531 701099236H1 SOYMON028 g534916 BLASTX 131 1e−10 75 7318 8531 700648547H1 SOYMON003 g534916 BLASTX 49 1e−9 57 7319 8531 700834052H1 SOYMON019 g534916 BLASTX 118 1e−9 92 7320 9059 700906027H1 SOYMON022 g2653445 BLASTN 1150 1e−86 94 7321 9059 700751263H1 SOYMON014 g2653445 BLASTN 1131 1e−85 95 7322 9059 701208611H1 SOYMON035 g2653445 BLASTN 666 1e−83 91 7323 9059 700832676H1 SOYMON019 g2653445 BLASTN 1078 1e−80 93 7324 9059 700979128H1 SOYMON009 g2653445 BLASTN 381 1e−71 90 7325 9059 700751040H1 SOYMON014 g2653445 BLASTN 872 1e−63 86 7326 9059 700957555H1 SOYMON022 g2653445 BLASTN 565 1e−40 86 7327 13047 LIB3028-012- LIB3028 g2653445 BLASTN 1120 1e−116 89 Q1-B1-B8 7328 13047 LIB3028-012- LIB3028 g2653445 BLASTN 1424 1e−115 91 Q1-B1-A6 7329 16 LIB3040-003- LIB3040 g633598 BLASTN 523 1e−51 74 Q1-E1-F6 7330 16 LIB3051-114- LIB3051 g790478 BLASTN 457 1e−48 79 Q1-K1-G5 7331 16 LIB3039-020- LIB3039 g790478 BLASTN 338 1e−30 74 Q1-E1-A2 7332 1820 LIB3065-010- LIB3065 g2653445 BLASTN 173 1e−10 88 Q1-N1-H3 7333 20885 LIB3051-070- LIB3051 g2653445 BLASTN 1058 1e−110 77 Q1-K1-B12 7334 27239 LIB3051-010- LIB3051 g1747293 BLASTN 544 1e−34 73 Q1-E1-G8 7335 2813 LIB3028-026- LIB3028 g2570500 BLASTN 1029 1e−77 80 Q1-B1-B7 7336 4845 LIB3039-007- LIB3039 g2653445 BLASTN 1826 1e−143 94 Q1-E1-H3 7337 4845 LIB3050-012- LIB3050 g2653445 BLASTN 1597 1e−124 91 Q1-E1-B11 7338 8040 LIB3049-005- LIB3049 g2570501 BLASTX 154 1e−32 61 Q1-E1-A7 7339 8531 LIB3050-013- LIB3050 g2570500 BLASTN 748 1e−53 72 Q1-E1-G8 7340 8531 LIB3073-025- LIB3073 g534915 BLASTN 711 1e−49 78 Q1-K1-D6 7341 8531 LIB3050-012- LIB3050 g2258074 BLASTX 93 1e−31 74 Q1-E1-D1

*Table Headings Cluster ID

A cluster ID is arbitrarily assigned to all of those clones which belong to the same cluster at a given stringency and a particular clone will belong to only one cluster at a given stringency. If a cluster contains only a single clone (a “singleton”), then the cluster ID number will be negative, with an absolute value equal to the clone ID number of its single member. The cluster ID entries in the table refer to the cluster with which the particular clone in each row is associated.

Clone ID

The clone ID number refers to the particular clone in the PhytoSeq database. Each clone ID entry in the table refers to the clone whose sequence is used for (1) the sequence comparison whose scores are presented and/or (2) assignment to the particular cluster which is presented. Note that a clone may be included in this table even if its sequence comparison scores fail to meet the minimum standards for similarity. In such a case, the clone is included due solely to its association with a particular cluster for which sequences of one or more other member clones possess the required level of similarity.

Library

The library ID refers to the particular cDNA library from which a given clone is obtained. Each cDNA library is associated with the particular tissue(s), line(s) and developmental stage(s) from which it is isolated.

NCBI gi

Each sequence in the GenBank public database is arbitrarily assigned a unique NCBI gi (National Center for Biotechnology Information GenBank Identifier) number. In this table, the NCBI gi number which is associated (in the same row) with a given clone refers to the particular GenBank sequence which is used in the sequence comparison. This entry is omitted when a clone is included solely due to its association with a particular cluster.

Method

The entry in the “Method” column of the table refers to the type of BLAST search that is used for the sequence comparison. “CLUSTER” is entered when the sequence comparison scores for a given clone fail to meet the minimum values required for significant similarity. In such cases, the clone is listed in the table solely as a result of its association with a given cluster for which sequences of one or more other member clones possess the required level of similarity.

Score

Each entry in the “Score” column of the table refers to the BLAST score that is generated by sequence comparison of the designated clone with the designated GenBank sequence using the designated BLAST method. This entry is omitted when a clone is included solely due to its association with a particular cluster. If the program used to determine the hit is HMMSW then the score refers to HMMSW score.

P-Value

The entries in the P-Value column refer to the probability that such matches occur by chance.

% Ident

The entries in the “% Ident” column of the table refer to the percentage of identically matched nucleotides (or residues) that exist along the length of that portion of the sequences which is aligned by the BLAST comparison to generate the statistical scores presented. This entry is omitted when a clone is included solely due to its association with a particular cluster. 

1-9. (canceled)
 10. A substantially purified nucleic acid molecule comprising a nucleic acid sequence wherein said nucleic acid sequence: (a) hybridizes under high stringency conditions to a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341, and a complete complement of SEQ ID NO: 1 through SEQ ID NO: 7341, or (b) shares at least 90% or greater identity to a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341, and a complete complement of SEQ ID NO: 1 through SEQ ID NO:
 7341. 11. The substantially purified nucleic acid molecule of claim 10, wherein said nucleic acid molecule encodes a maize or soybean carbon assimilation pathway enzyme.
 12. A substantially purified nucleic acid molecule comprising a nucleic acid sequence that shares between 100% and 90% sequence identity with a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341 and a complete complement of SEQ ID NO: 1 through SEQ ID NO:
 7341. 13. The substantially purified nucleic acid molecule of claim 12, wherein said nucleic acid sequence shares between 100% and 95% sequence identity with a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341 and a complete complement of SEQ ID NO: 1 through SEQ ID NO:
 7341. 14. The substantially purified nucleic, acid molecule of claim 13, wherein said nucleic acid sequence shares between 100% and 98% sequence identity with a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341 and a complete complement of SEQ ID NO: 1 through SEQ ID NO:
 7341. 15. The substantially purified nucleic acid molecule of claim 14, wherein said nucleic acid sequence shares between 100% and 99% sequence identity with a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341 and a complete complement of SEQ ID NO: 1 through SEQ ID NO:
 7341. 16. The substantially purified nucleic acid molecule of claim 15, wherein said nucleic acid sequence exhibits 100% sequence identity with a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341 and a complete complement of SEQ ID NO: 1 through SEQ ID NO:
 7341. 17. A substantially purified polypeptide, wherein said polypeptide is encoded by a nucleic acid molecule comprising a nucleic acid sequence, wherein said nucleic acid sequence: (a) hybridizes under high stringency conditions to a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341 and a complete complement of SEQ ID NO: 1 through SEQ ID NO: 7341, or (b) shares at least 90% or greater identity to a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341 and a complete complement of SEQ ID NO: 1 through SEQ ID NO:
 7341. 18. A transformed plant comprising a nucleic acid molecule which comprises: (a) an exogenous promoter region which functions in a plant cell to cause the production of an mRNA molecule; which is linked to; (b) a structural nucleic acid molecule, wherein said structural nucleic acid molecule comprises a nucleic acid sequence, wherein said nucleic acid sequence (i) hybridizes under high stringency conditions to a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341 and a complete complement of SEQ ID NO: 1 through SEQ ID NO: 7341; or (ii) shares at least 90% or greater identity to a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341 and a complete complement of SEQ ID NO: 1 through SEQ ID NO: 7341, or which is linked to (c) a 3′ non-translated sequence that functions in said plant cell to cause the termination of transcription and the addition of polyadenylated ribonucleotides to said 3′ end of said mRNA molecule.
 19. The transformed plant according to claim 18, wherein said nucleic acid sequence is a complete complement of a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO:
 7341. 20. The transformed plant according to claim 19, wherein said plant is selected from the group consisting of cotton, soybean, maize and wheat.
 21. The transformed plant according to claim 20, wherein said plant is cotton.
 22. The transformed plant according to claim 20, wherein said plant is soybean.
 23. The transformed plant according to claim 20, wherein said plant is maize.
 24. The transformed plant according to claim 20, wherein said plant is wheat.
 25. A transformed seed comprising a transformed plant cell comprising a nucleic acid molecule which comprises: (a) an exogenous promoter region which functions in said plant cell to cause the production of an mRNA molecule; which is linked to; (b) a structural nucleic acid molecule, wherein said structural nucleic acid molecule comprises a nucleic acid sequence, wherein said nucleic acid sequence (i) hybridizes under high stringency conditions to a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341, and a complete complement of SEQ ID NO: 1 through SEQ ID NO: 7341; or (ii) shares at least a 90% or greater identity to a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341, and a complete complement of SEQ ID NO: 1 through SEQ ID NO: 7341, which is linked to (c) a 3′ non-translated sequence that functions in said plant cell to cause the termination of transcription and the addition of polyadenylated ribonucleotides to said 3′ end of said mRNA molecule.
 26. The transformed seed according to claim 25, wherein said nucleic acid sequence is a complete complement of a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO:
 7341. 27. The transformed seed according to claim 25, wherein said exogenous promoter region functions in a seed cell.
 28. The transformed seed according to claim 25, wherein said seed is selected from the group consisting of a cotton, soybean, maize and wheat seed.
 29. The transformed seed according to claim 28, wherein said seed is a cotton seed.
 30. The transformed seed according to claim 28, wherein said seed is a soybean seed.
 31. The transformed seed according to claim 28, wherein said seed is a maize seed.
 32. The transformed seed according to claim 28, wherein said seed is a wheat seed.
 33. A method of producing a genetically transformed plant, comprising the steps of: (a) inserting into the genome of a plant cell a recombinant, double-stranded DNA molecule comprising (i) a promoter which functions in a plant cell to cause the production of an RNA sequence, (ii) a structural nucleic acid molecule, wherein said structural nucleic acid molecule comprises a nucleic acid sequence, wherein said nucleic acid sequence (A) hybridizes under high stringency conditions to a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341, and a complete complement of SEQ ID NO: 1 through SEQ ID NO: 7341; or (B) shares at least a 90% or greater identity to a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341 and a complete complement of SEQ ID NO: 1 through SEQ ID NO: 7341, which is linked to (iii) a 3′ non-translated sequence which functions in plant cells to cause the addition of polyadenylated nucleotides to the 3′ end of RNA sequence, (b) obtaining a transformed plant cell with said structural nucleic acid molecule that encodes one or more proteins, wherein said structural nucleic acid molecule is transcribed and results in expression of said protein(s); and (c) regenerating from said transformed plant cell a genetically transformed plant.
 34. A method for reducing expression of a protein in a plant cell comprising growing a transformed plant cell containing a nucleic acid molecule wherein the non-transcribed strand of said nucleic acid molecule encodes a protein or fragment thereof, and wherein the transcribed strand of said nucleic acid molecule is complementary to a nucleic acid molecule comprising a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341, and a complete complement of SEQ ID NO: 1 through SEQ ID NO: 7341, and whereby said transcribed strand reduces or depresses expression of said protein.
 35. A method for causing overexpression of a protein in a plant cell comprising growing a transformed plant cell containing a nucleic acid molecule that encodes a protein or fragment thereof, wherein said nucleic acid molecule comprises a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341, and a complete complement of SEQ ID NO: 1 through SEQ ID NO: 7341, and whereby said nucleic acid molecule increases expression of said protein.
 36. A method of producing a plant containing reduced levels of a protein comprising: (a) transforming a plant cell with a nucleic acid molecule comprising a nucleic acid sequence selected from the group consisting of SEQ ID NO:1 through SEQ ID NO: 7341, and a complete complement of SEQ ID NO: 1 through SEQ ID NO: 7341, wherein said nucleic acid molecule is transcribed and results in decreased expression or co-suppression of endogenous protein synthesis activity, and (b) regenerating said plant comprising said plant cell and producing subsequent progeny from said plant.
 37. A method of growing a transgenic plant comprising (a) planting a transformed seed comprising a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1 through SEQ ID NO: 7341, and a complete complement of SEQ ID NO: 1 through SEQ ID NO: 7341, and (b) growing a plant from said seed. 